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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093777copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,283,594-102,510,668 , GRCh38.p12 chr10: 100,523,837-100,750,911 NDUFB8, PAX2, 1 more genes
    nsv7076061inversion1nstd229human GRCh38 chr10: 100,560,059-100,568,038 , GRCh37.p13 chr10: 102,319,816-102,327,795 HIF1AN
    nsv7064309inversion1nstd229human GRCh38 chr10: 100,500,702-100,949,925 , GRCh37.p13 chr10: 102,260,459-102,709,682 HIF1AN, NDUFB8, 3 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6895337copy number variation1nstd229human GRCh38 chr10: 100,549,254-100,549,444 , GRCh37.p13 chr10: 102,309,011-102,309,201 HIF1AN
    nsv6887253copy number variation1nstd229human GRCh38 chr10: 100,544,912-100,568,591 , GRCh37.p13 chr10: 102,304,669-102,328,348 HIF1AN
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6453002copy number variation1nstd223human GRCh38 chr10: 100,512,435-100,608,282 , GRCh37.p13 chr10: 102,272,192-102,368,039 HIF1AN, SEC31B, 1 more genes
    nsv6442165copy number variation1nstd223human GRCh38 chr10: 100,550,896-100,551,414 , GRCh37.p13 chr10: 102,310,653-102,311,171 HIF1AN
    nsv6247433mobile element insertion1nstd215human GRCh38 chr10: 100,542,869-100,542,869 , GRCh37.p13 chr10: 102,302,626-102,302,626 HIF1AN
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv5723929mobile element insertion1nstd211human GRCh38 chr10: 100,535,337-100,535,337 , GRCh37.p13 chr10: 102,295,094-102,295,094 HIF1AN
    nsv5711874mobile element insertion1nstd211human GRCh38 chr10: 100,542,869-100,542,869 , GRCh37.p13 chr10: 102,302,626-102,302,626 HIF1AN
    nsv5705664mobile element insertion2nstd211human GRCh38 chr10: 100,554,008-100,554,008 , GRCh37.p13 chr10: 102,313,765-102,313,765 HIF1AN
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