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Items: 1 to 20 of 313

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077577inversion1nstd229human GRCh38 chr13: 20,751,593-20,758,609 , GRCh37.p13 chr13: 21,325,732-21,332,748 EEF1AKMT1
    nsv7073256inversion1nstd229human GRCh38 chr13: 19,714,497-24,851,015 , GRCh37.p13 chr13: 20,288,637-25,425,153 SPATA13, IFT88, 114 more genes
    nsv7072424inversion1nstd229human GRCh38 chr13: 20,061,787-21,405,901 , GRCh37.p13 chr13: 20,635,927-21,980,040 IPPKP1, CRYL1, 41 more genes
    nsv7071368inversion1nstd229human GRCh38 chr13: 19,560,696-21,260,853 , GRCh37.p13 chr13: 20,134,836-21,834,992 ZMYM2, EEF1AKMT1, 44 more genes
    nsv7071034inversion1nstd229human GRCh38 chr13: 19,239,514-24,381,508 , GRCh37.p13 chr13: 19,813,654-24,955,646 BASP1P1, ZMYM5, 111 more genes
    nsv7068264inversion1nstd229human GRCh38 chr13: 20,443,147-22,597,794 , GRCh37.p13 chr13: 21,017,286-23,171,933 RPSAP54, IL17D, 43 more genes
    nsv7067925inversion1nstd229human GRCh38 chr13: 19,527,899-24,671,591 , GRCh37.p13 chr13: 20,102,039-25,245,729 TPTE2-AS1, TNFRSF19, 112 more genes
    nsv7065933inversion1nstd229human GRCh38 chr13: 19,560,717-21,260,795 , GRCh37.p13 chr13: 20,134,857-21,834,934 LOC105370101, GJB2, 44 more genes
    nsv7065531inversion1nstd229human GRCh38 chr13: 20,507,648-21,110,224 , GRCh37.p13 chr13: 21,081,787-21,684,363 HNRNPA1P30, XPO4, 17 more genes
    nsv7061961inversion1nstd229human GRCh38 chr13: 20,241,182-21,970,619 , GRCh37.p13 chr13: 20,815,321-22,544,758 RNA5SP25, CRYL1, 40 more genes
    nsv7058292inversion1nstd229human GRCh38 chr13: 19,736,413-23,270,103 , GRCh37.p13 chr13: 20,310,553-23,844,242 PPIAP28, RPL7AP73, 75 more genes
    nsv6932713copy number variation1nstd229human GRCh38 chr13: 19,442,684-24,587,300 , GRCh37.p13 chr13: 20,016,824-25,161,438 CEND1P2, MTCO3P2, 112 more genes
    nsv6929556copy number variation1nstd229human GRCh38 chr13: 20,726,028-20,746,446 , GRCh37.p13 chr13: 21,300,167-21,320,585 EEF1AKMT1, RANP8
    nsv6925163copy number variation1nstd229human GRCh38 chr13: 20,732,601-20,753,765 , GRCh37.p13 chr13: 21,306,740-21,327,904 EEF1AKMT1, RANP8
    nsv6923379copy number variation1nstd229human GRCh38 chr13: 20,711,201-20,740,800 , GRCh37.p13 chr13: 21,285,340-21,314,939 IL17D, EEF1AKMT1
    nsv6637646copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,287-22,089,005 , GRCh38.p12 chr13: 18,862,147-21,514,866 LOC105370104, RNU6-52P, 78 more genes
    nsv6637390copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,436,287-22,405,375 , GRCh38.p12 chr13: 18,862,147-21,831,236 SLC35E1P1, LOC107984553, 83 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6595178inversion1nstd223human GRCh38 chr13: 19,560,915-21,260,707 , GRCh37.p13 chr13: 20,135,055-21,834,846 TPTE2-AS1, GJB2, 44 more genes
    nsv6591798inversion1nstd223human GRCh38 chr13: 20,748,233-20,748,719 , GRCh37.p13 chr13: 21,322,372-21,322,858 EEF1AKMT1, RANP8
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