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nsv4348764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:25,363,180
  • Description:GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095) AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 72423 SVs from 140 studies. See in: genome view    
Remapped(Score: Good):108,262,412-133,625,591Question Mark
Overlapping variant regions from other studies: 71961 SVs from 140 studies. See in: genome view    
Submitted genomic110,022,170-135,439,095Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4348764RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10108,262,412133,625,591
nsv4348764Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10110,022,170135,439,095

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15605860copy number gainMultipleMultiplenot providedPathogenicClinVarRCV000767665.1, VCV000625657.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15605860RemappedGoodNC_000010.11:g.(?_
108262412)_(133625
591_?)dup
GRCh38.p12First PassNC_000010.11Chr10108,262,412133,625,591
nssv15605860Submitted genomicNC_000010.10:g.(?_
110022170)_(135439
095_?)dup
GRCh37 (hg19)NC_000010.10Chr10110,022,170135,439,095

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15605860GRCh37: NC_000010.10:g.(?_110022170)_(135439095_?)dupcopy number gaingermlinenot providedPathogenicClinVarRCV000767665.1, VCV000625657.1

No genotype data were submitted for this variant

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