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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv7050608inversion1nstd229human GRCh38 chr6: 83,630,811-83,741,751 , GRCh37.p13 chr6: 84,340,530-84,451,470 SNAP91, LOC105377879
    nsv6816854copy number variation1nstd229human GRCh38 chr6: 83,298,441-83,971,760 , GRCh37.p13 chr6: 84,008,160-84,681,479 RIPPLY2, ME1, 4 more genes
    nsv6816698copy number variation1nstd229human GRCh38 chr6: 83,623,147-83,623,397 , GRCh37.p13 chr6: 84,332,866-84,333,116 SNAP91
    nsv6815208copy number variation1nstd229human GRCh38 chr6: 83,648,150-83,653,807 , GRCh37.p13 chr6: 84,357,869-84,363,526 SNAP91
    nsv6814886copy number variation1nstd229human GRCh38 chr6: 83,667,037-83,667,237 , GRCh37.p13 chr6: 84,376,756-84,376,956 SNAP91
    nsv6806571copy number variation1nstd229human GRCh38 chr6: 83,566,464-83,569,069 , GRCh37.p13 chr6: 84,276,183-84,278,788 SNAP91
    nsv6804320copy number variation1nstd229human GRCh38 chr6: 83,705,344-83,705,385 , GRCh37.p13 chr6: 84,415,063-84,415,104 SNAP91
    nsv6801339copy number variation1nstd229human GRCh38 chr6: 83,692,201-83,815,100 , GRCh37.p13 chr6: 84,401,920-84,524,819 LOC105377879, SNAP91
    nsv6799418copy number variation1nstd229human GRCh38 chr6: 83,432,892-83,647,787 , GRCh37.p13 chr6: 84,142,611-84,357,506 PRSS35, SNAP91
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6636520copy number variation1nstd102humanUncertain significance GRCh37 chr6: 84,373,743-85,044,270 , GRCh38.p12 chr6: 83,664,024-84,334,552 CYB5R4, CEP162, 5 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6572504inversion1nstd223human GRCh38 chr6: 83,658,035-83,658,395 , GRCh37.p13 chr6: 84,367,754-84,368,114 SNAP91
    nsv6570207inversion1nstd223human GRCh38 chr6: 83,611,849-83,612,820 , GRCh37.p13 chr6: 84,321,568-84,322,539 SNAP91
    nsv6563283inversion1nstd223human GRCh38 chr6: 83,497,722-83,901,118 , GRCh37.p13 chr6: 84,207,441-84,610,837 SNAP91, CYB5R4, 3 more genes
    nsv6415575copy number variation1nstd223human GRCh38 chr6: 83,684,739-83,685,817 , GRCh37.p13 chr6: 84,394,458-84,395,536 SNAP91
    nsv6415267copy number variation1nstd223human GRCh38 chr6: 83,694,155-83,694,558 , GRCh37.p13 chr6: 84,403,874-84,404,277 SNAP91
    nsv6413906copy number variation1nstd223human GRCh38 chr6: 83,562,642-83,563,260 , GRCh37.p13 chr6: 84,272,361-84,272,979 SNAP91
    nsv6413715copy number variation1nstd223human GRCh38 chr6: 83,654,543-83,654,988 , GRCh37.p13 chr6: 84,364,262-84,364,707 SNAP91
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