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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7064456inversion1nstd229human GRCh38 chr8: 102,463,034-102,788,786 , GRCh37.p13 chr8: 103,475,262-103,801,014 KLF10, LOC105375685, 10 more genes
    nsv7062210inversion1nstd229human GRCh38 chr8: 102,582,626-102,990,892 , GRCh37.p13 chr8: 103,594,854-104,003,120 LOC105375685, KLF10, 8 more genes
    nsv6853485copy number variation1nstd229human GRCh38 chr8: 102,647,725-102,650,049 , GRCh37.p13 chr8: 103,659,953-103,662,277 KLF10
    nsv6844720copy number variation1nstd229human GRCh38 chr8: 102,645,601-102,654,400 , GRCh37.p13 chr8: 103,657,829-103,666,628 KLF10, LOC101927245
    nsv6637853copy number variation1nstd102humanUncertain significance GRCh37 chr8: 103,625,216-103,830,188 , GRCh38.p12 chr8: 102,612,988-102,817,960 GASAL1, LOC101927245, 5 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6312665copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,135,566-106,815,766 , GRCh38.p12 chr8: 98,123,338-105,803,538 RNU6-748P, RN7SKP85, 144 more genes
    nsv6137031copy number variation1nstd213human GRCh37 chr8: 103,400,000-104,040,001 , GRCh38.p12 chr8: 102,387,772-103,027,773 ADI1P2, MAILR, 19 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136226copy number variation1nstd213human GRCh37 chr8: 103,400,000-104,860,001 , GRCh38.p12 chr8: 102,387,772-103,847,773 KLF10, RIMS2, 41 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6135809copy number variation1nstd213human GRCh37 chr8: 103,320,000-121,640,001 , GRCh38.p12 chr8: 102,307,772-120,627,761 TNFRSF11B, RAD21, 186 more genes
    nsv5486283copy number variation1nstd206human GRCh38 chr8: 102,655,881-102,655,933 , GRCh37.p13 chr8: 103,668,109-103,668,161 LOC101927245, KLF10
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