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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6916343copy number variation1nstd229human GRCh38 chr11: 75,604,241-75,604,803 , GRCh37.p13 chr11: 75,315,286-75,315,848 MAP6
    nsv6915604copy number variation1nstd229human GRCh38 chr11: 75,626,075-75,626,156 , GRCh37.p13 chr11: 75,337,120-75,337,201 MAP6
    nsv6914661copy number variation1nstd229human GRCh38 chr11: 75,633,149-75,633,515 , GRCh37.p13 chr11: 75,344,194-75,344,560 MAP6
    nsv6913669copy number variation1nstd229human GRCh38 chr11: 75,627,057-75,630,165 , GRCh37.p13 chr11: 75,338,102-75,341,210 MAP6
    nsv6911312copy number variation1nstd229human GRCh38 chr11: 75,586,982-75,590,570 , GRCh37.p13 chr11: 75,298,027-75,301,615 LOC105369391, MAP6
    nsv6910876copy number variation1nstd229human GRCh38 chr11: 75,635,201-75,639,200 , GRCh37.p13 chr11: 75,346,246-75,350,245 MAP6
    nsv6910444copy number variation1nstd229human GRCh38 chr11: 75,621,313-75,626,794 , GRCh37.p13 chr11: 75,332,358-75,337,839 MAP6
    nsv6906946copy number variation1nstd229human GRCh38 chr11: 75,240,901-75,668,300 , GRCh37.p13 chr11: 74,951,946-75,379,345 LOC105369389, LOC100419542, 11 more genes
    nsv6905812copy number variation1nstd229human GRCh38 chr11: 75,635,140-75,639,221 , GRCh37.p13 chr11: 75,346,185-75,350,266 MAP6
    nsv6904924copy number variation1nstd229human GRCh38 chr11: 75,591,613-75,592,223 , GRCh37.p13 chr11: 75,302,658-75,303,268 LOC105369391, MAP6
    nsv6901641copy number variation1nstd229human GRCh38 chr11: 75,587,001-75,590,500 , GRCh37.p13 chr11: 75,298,046-75,301,545 LOC105369391, MAP6
    nsv6899215copy number variation1nstd229human GRCh38 chr11: 75,042,869-75,776,821 , GRCh37.p13 chr11: 74,753,914-75,487,866 DGAT2, LOC100421207, 25 more genes
    nsv6595007inversion1nstd223human GRCh38 chr11: 75,646,540-75,647,252 , GRCh37.p13 chr11: 75,357,585-75,358,297 MAP6
    nsv6464395copy number variation1nstd223human GRCh38 chr11: 75,660,518-75,660,958 , GRCh37.p13 chr11: 75,371,563-75,372,003 MAP6
    nsv6461916copy number variation1nstd223human GRCh38 chr11: 75,591,582-75,592,279 , GRCh37.p13 chr11: 75,302,627-75,303,324 LOC105369391, MAP6
    nsv6458719copy number variation1nstd223human GRCh38 chr11: 75,586,982-75,590,566 , GRCh37.p13 chr11: 75,298,027-75,301,611 MAP6, LOC105369391
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314051copy number variation1nstd102humanUncertain significance GRCh37 chr11: 74,839,014-75,366,449 , GRCh38.p12 chr11: 75,127,969-75,655,404 LOC107984358, KLHL35, 16 more genes
    nsv6203708copy number variation1nstd214human GRCh38 chr11: 75,626,075-75,626,155 , GRCh37.p13 chr11: 75,337,120-75,337,200 MAP6
    nsv6132278copy number variation1nstd213human GRCh37 chr11: 75,150,000-75,550,001 , GRCh38.p12 chr11: 75,438,955-75,838,956 MAP6, DGAT2, 11 more genes
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