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esv3474874

  • Variant Calls:24
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:36,515

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 198 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):104,324,780-104,361,314Question Mark
Overlapping variant regions from other studies: 198 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):104,772,655-104,809,189Question Mark
Overlapping variant regions from other studies: 61 SVs from 12 studies. See in: genome view    
Submitted genomic104,879,348-104,915,882Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3474874RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
esv3474874RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
esv3474874Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7682774deletionSAMN00001604SequencingSplit read mapping13,004
essv7682776deletionSAMN00801027SequencingSplit read mapping12,816
essv7682777deletionSAMN00001660SequencingSplit read mapping13,045
essv7682778deletionSAMN00001665SequencingSplit read mapping11,494
essv7682779deletionSAMN00797126SequencingSplit read mapping11,843
essv7682780deletionSAMN00001668SequencingSplit read mapping11,562
essv7682781deletionSAMN00001605SequencingSplit read mapping14,569
essv7682782deletionSAMN00001564SequencingSplit read mapping9,310
essv7682783deletionSAMN00001666SequencingSplit read mapping11,359
essv7682784deletionSAMN00801031SequencingSplit read mapping9,208
essv7682785deletionSAMN00001671SequencingSplit read mapping10,275
essv7682787deletionSAMN00001644SequencingSplit read mapping14,069
essv7682788deletionSAMN00001593SequencingSplit read mapping15,444
essv7682789deletionSAMN00001648SequencingSplit read mapping15,747
essv7682790deletionSAMN00001584SequencingSplit read mapping11,452
essv7682791deletionSAMN00001600SequencingSplit read mapping15,861
essv7682792deletionSAMN00001667SequencingSplit read mapping12,201
essv7682793deletionSAMN00001647SequencingSplit read mapping26,594
essv7682794deletionSAMN00001624SequencingSplit read mapping10,264
essv7682795deletionSAMN00001639SequencingSplit read mapping14,223
essv7682796deletionSAMN00001597SequencingSplit read mapping14,192
essv7682798deletionSAMN00801680SequencingSplit read mapping19,937
essv7682799deletionSAMN00801646SequencingSplit read mapping11,757
essv7682800deletionSAMN00001596SequencingSplit read mapping14,505

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv7682774RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682776RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682777RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682778RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682779RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682780RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682781RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682782RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682783RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682784RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682785RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682787RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682788RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682789RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682790RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682791RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682792RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682793RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682794RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682795RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682796RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682798RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682799RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682800RemappedPerfectNC_000006.12:g.(10
4324780_104324800)
_(104361295_104361
314)del
GRCh38.p12First PassNC_000006.12Chr6104,324,795 (-15, +5)104,361,309 (-14, +5)
essv7682774RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682776RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682777RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682778RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682779RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682780RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682781RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682782RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682783RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682784RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682785RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682787RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682788RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682789RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682790RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682791RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682792RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682793RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682794RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682795RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682796RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682798RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682799RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682800RemappedPerfectNC_000006.11:g.(10
4772655_104772675)
_(104809170_104809
189)del
GRCh37.p13First PassNC_000006.11Chr6104,772,670 (-15, +5)104,809,184 (-14, +5)
essv7682774Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682776Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682777Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682778Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682779Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682780Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682781Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682782Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682783Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682784Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682785Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682787Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682788Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682789Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682790Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682791Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682792Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682793Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682794Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682795Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682796Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682798Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682799Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)
essv7682800Submitted genomicNC_000006.10:g.(10
4879348_104879368)
_(104915863_104915
882)del
NCBI36 (hg18)NC_000006.10Chr6104,879,363 (-15, +5)104,915,877 (-14, +5)

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv768278236SAMN00001564Digital arrayOtherFail
essv768278238SAMN00001564Digital arrayOtherFail
essv768279036SAMN00001584Digital arrayOtherFail
essv768279038SAMN00001584Digital arrayOtherFail
essv768278836SAMN00001593Digital arrayOtherFail
essv768278838SAMN00001593Digital arrayOtherFail
essv768280036SAMN00001596Digital arrayOtherFail
essv768280038SAMN00001596Digital arrayOtherFail
essv768279636SAMN00001597Digital arrayOtherFail
essv768279638SAMN00001597Digital arrayOtherFail
essv768279136SAMN00001600Digital arrayOtherFail
essv768279138SAMN00001600Digital arrayOtherFail
essv768277436SAMN00001604Digital arrayOtherFail
essv768277438SAMN00001604Digital arrayOtherFail
essv768278136SAMN00001605Digital arrayOtherFail
essv768278138SAMN00001605Digital arrayOtherFail
essv768279436SAMN00001624Digital arrayOtherFail
essv768279438SAMN00001624Digital arrayOtherFail
essv768279536SAMN00001639Digital arrayOtherFail
essv768279538SAMN00001639Digital arrayOtherFail
essv768278736SAMN00001644Digital arrayOtherFail
essv768278738SAMN00001644Digital arrayOtherFail
essv768279336SAMN00001647Digital arrayOtherFail
essv768279338SAMN00001647Digital arrayOtherFail
essv768278936SAMN00001648Digital arrayOtherFail
essv768278938SAMN00001648Digital arrayOtherFail
essv768277736SAMN00001660Digital arrayOtherFail
essv768277738SAMN00001660Digital arrayOtherFail
essv768277836SAMN00001665Digital arrayOtherFail
essv768277838SAMN00001665Digital arrayOtherFail
essv768278336SAMN00001666Digital arrayOtherFail
essv768278338SAMN00001666Digital arrayOtherFail
essv768279236SAMN00001667Digital arrayOtherFail
essv768279238SAMN00001667Digital arrayOtherFail
essv768278036SAMN00001668Digital arrayOtherFail
essv768278038SAMN00001668Digital arrayOtherFail
essv768278536SAMN00001671Digital arrayOtherFail
essv768278538SAMN00001671Digital arrayOtherFail
essv768277936SAMN00797126Digital arrayOtherFail
essv768277938SAMN00797126Digital arrayOtherFail
essv768277636SAMN00801027Digital arrayOtherFail
essv768277638SAMN00801027Digital arrayOtherFail
essv768278436SAMN00801031Digital arrayOtherFail
essv768278438SAMN00801031Digital arrayOtherFail
essv768279936SAMN00801646Digital arrayOtherFail
essv768279938SAMN00801646Digital arrayOtherFail
essv768279836SAMN00801680Digital arrayOtherFail
essv768279838SAMN00801680Digital arrayOtherFail
essv768278237SAMN00001564Sequencingde novo sequence assemblyPass
essv768279037SAMN00001584Sequencingde novo sequence assemblyPass
essv768278837SAMN00001593Sequencingde novo sequence assemblyPass
essv768280037SAMN00001596Sequencingde novo sequence assemblyPass
essv768279637SAMN00001597Sequencingde novo sequence assemblyPass
essv768279137SAMN00001600Sequencingde novo sequence assemblyPass
essv768277437SAMN00001604Sequencingde novo sequence assemblyPass
essv768278137SAMN00001605Sequencingde novo sequence assemblyPass
essv768279437SAMN00001624Sequencingde novo sequence assemblyPass
essv768279537SAMN00001639Sequencingde novo sequence assemblyPass
essv768278737SAMN00001644Sequencingde novo sequence assemblyPass
essv768279337SAMN00001647Sequencingde novo sequence assemblyPass
essv768278937SAMN00001648Sequencingde novo sequence assemblyPass
essv768277737SAMN00001660Sequencingde novo sequence assemblyPass
essv768277837SAMN00001665Sequencingde novo sequence assemblyPass
essv768278337SAMN00001666Sequencingde novo sequence assemblyPass
essv768279237SAMN00001667Sequencingde novo sequence assemblyPass
essv768278037SAMN00001668Sequencingde novo sequence assemblyPass
essv768278537SAMN00001671Sequencingde novo sequence assemblyPass
essv768277937SAMN00797126Sequencingde novo sequence assemblyPass
essv768277637SAMN00801027Sequencingde novo sequence assemblyPass
essv768278437SAMN00801031Sequencingde novo sequence assemblyPass
essv768279937SAMN00801646Sequencingde novo sequence assemblyPass
essv768279837SAMN00801680Sequencingde novo sequence assemblyPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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