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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114295mobile element insertion1nstd186human GRCh37 chr12: 118,461,600-118,461,651 , GRCh38.p12 chr12: 118,023,795-118,023,846 RFC5
    nsv5977092insertion1nstd209human GRCh38 chr12: 118,023,781-118,023,781 , GRCh37.p13 chr12: 118,461,586-118,461,586 RFC5
    nsv5946730copy number variation1nstd209human GRCh38 chr12: 118,024,022-118,024,144 , GRCh37.p13 chr12: 118,461,827-118,461,949 RFC5
    nsv5724757mobile element insertion1nstd211human GRCh38 chr12: 118,032,093-118,032,093 , GRCh37.p13 chr12: 118,469,898-118,469,898 RFC5, WSB2
    nsv5702911mobile element insertion2nstd211human GRCh38 chr12: 118,023,795-118,023,795 , GRCh37.p13 chr12: 118,461,600-118,461,600 RFC5
    nsv5661231insertion1nstd207human GRCh38 chr12: 118,023,781-118,023,781 , GRCh37.p13 chr12: 118,461,586-118,461,586 RFC5
    nsv5421405mobile element insertion1nstd206human GRCh38 chr12: 118,023,795-118,023,846 , GRCh37.p13 chr12: 118,461,600-118,461,651 RFC5
    nsv5136743mobile element insertion1nstd203human GRCh38 chr12: 118,023,786-118,023,795 , GRCh37.p13 chr12: 118,461,591-118,461,600 RFC5
    nsv5135843mobile element insertion1nstd203human GRCh38 chr12: 118,023,788-118,023,795 , GRCh37.p13 chr12: 118,461,593-118,461,600 RFC5
    nsv5135144mobile element insertion1nstd203human GRCh38 chr12: 118,023,780-118,023,795 , GRCh37.p13 chr12: 118,461,585-118,461,600 RFC5
    nsv5133482mobile element insertion1nstd203human GRCh38 chr12: 118,023,781-118,023,795 , GRCh37.p13 chr12: 118,461,586-118,461,600 RFC5
    nsv5132538mobile element insertion1nstd203human GRCh38 chr12: 118,023,795-118,023,801 , GRCh37.p13 chr12: 118,461,600-118,461,606 RFC5
    nsv5122489mobile element insertion1nstd203human GRCh38 chr12: 118,023,785-118,023,795 , GRCh37.p13 chr12: 118,461,590-118,461,600 RFC5
    nsv5120213mobile element insertion1nstd203human GRCh38 chr12: 118,023,784-118,023,795 , GRCh37.p13 chr12: 118,461,589-118,461,600 RFC5
    nsv4995871copy number variation1nstd200human GRCh38 chr12: 118,016,632-118,024,553 , GRCh37.p13 chr12: 118,454,437-118,462,358 RFC5
    nsv4993733copy number variation1nstd200human GRCh38 chr12: 118,010,490-118,022,001 , GRCh37.p13 chr12: 118,448,295-118,459,806 RFC5
    nsv4829550copy number variation1nstd200human GRCh37 chr12: 118,460,372-118,463,717 , GRCh38.p12 chr12: 118,022,567-118,025,912 RFC5
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
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