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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7094241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,442,029-105,861,009 , GRCh38.p12 chr14: 101,975,692-105,394,672 LOC107984670, MARK3, 101 more genes
    nsv7094007copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,228,231-105,861,009 , GRCh38.p12 chr14: 101,761,894-105,394,672 CLBA1, BAG5, 105 more genes
    nsv7065244inversion1nstd229human GRCh38 chr14: 102,274,162-102,275,257 , GRCh37.p13 chr14: 102,740,499-102,741,594 MOK
    nsv7060610inversion1nstd229human GRCh38 chr14: 102,225,051-102,225,158 , GRCh37.p13 chr14: 102,691,388-102,691,495 WDR20, MOK
    nsv6977173copy number variation1nstd229human GRCh38 chr14: 102,234,701-102,273,100 , GRCh37.p13 chr14: 102,701,038-102,739,437 MOK
    nsv6977041copy number variation1nstd229human GRCh38 chr14: 102,244,941-102,251,566 , GRCh37.p13 chr14: 102,711,278-102,717,903 MOK
    nsv6975863copy number variation1nstd229human GRCh38 chr14: 102,246,801-102,249,300 , GRCh37.p13 chr14: 102,713,138-102,715,637 MOK
    nsv6974570copy number variation1nstd229human GRCh38 chr14: 102,252,070-102,257,466 , GRCh37.p13 chr14: 102,718,407-102,723,803 MOK
    nsv6973709copy number variation1nstd229human GRCh38 chr14: 102,267,065-102,272,927 , GRCh37.p13 chr14: 102,733,402-102,739,264 MOK
    nsv6973592copy number variation1nstd229human GRCh38 chr14: 102,239,370-102,239,438 , GRCh37.p13 chr14: 102,705,707-102,705,775 MOK
    nsv6973308copy number variation1nstd229human GRCh38 chr14: 102,226,795-102,231,628 , GRCh37.p13 chr14: 102,693,132-102,697,965 MOK
    nsv6971556copy number variation1nstd229human GRCh38 chr14: 102,223,605-102,239,656 , GRCh37.p13 chr14: 102,689,942-102,705,993 MOK, WDR20
    nsv6970258copy number variation1nstd229human GRCh38 chr14: 102,273,486-102,298,955 , GRCh37.p13 chr14: 102,739,823-102,765,292 MOK
    nsv6969794copy number variation1nstd229human GRCh38 chr14: 102,207,096-102,319,544 , GRCh37.p13 chr14: 102,673,433-102,785,881 TRI-AAT5-4, WDR20, 2 more genes
    nsv6969398copy number variation1nstd229human GRCh38 chr14: 102,274,245-102,278,332 , GRCh37.p13 chr14: 102,740,582-102,744,669 MOK
    nsv6969196copy number variation1nstd229human GRCh38 chr14: 102,273,706-102,285,839 , GRCh37.p13 chr14: 102,740,043-102,752,176 MOK
    nsv6969186copy number variation1nstd229human GRCh38 chr14: 102,302,577-102,330,429 , GRCh37.p13 chr14: 102,768,914-102,796,766 TRI-AAT5-4, ZNF839, 1 more genes
    nsv6968131copy number variation1nstd229human GRCh38 chr14: 102,202,687-102,283,029 , GRCh37.p13 chr14: 102,669,024-102,749,366 LOC105370677, MOK, 1 more genes
    nsv6967873copy number variation1nstd229human GRCh38 chr14: 102,278,363-102,282,343 , GRCh37.p13 chr14: 102,744,700-102,748,680 MOK
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