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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974989inversion1nstd209human GRCh38 chr11: 112,292,844-112,293,167 , GRCh37.p13 chr11: 112,163,567-112,163,890 LINC02762
    nsv5925945copy number variation1nstd209human GRCh38 chr11: 112,334,657-112,336,474 , GRCh37.p13 chr11: 112,205,380-112,207,197 LOC107984388, LINC02762
    nsv5916807copy number variation1nstd209human GRCh38 chr11: 112,331,777-112,331,914 , GRCh37.p13 chr11: 112,202,500-112,202,637 LINC02762
    nsv5853425copy number variation1nstd209human GRCh38 chr11: 112,293,011-112,297,919 , GRCh37.p13 chr11: 112,163,734-112,168,642 LINC02762
    nsv5731023mobile element insertion1nstd211human GRCh38 chr11: 112,344,643-112,344,643 , GRCh37.p13 chr11: 112,215,366-112,215,366 LINC02762
    nsv5659972insertion1nstd207human GRCh38 chr11: 112,331,793-112,331,793 , GRCh37.p13 chr11: 112,202,516-112,202,516 LINC02762
    nsv5560658sequence alteration1nstd206human GRCh38 chr11: 112,292,849-112,297,885 , GRCh37.p13 chr11: 112,163,572-112,168,608 LINC02762
    nsv5554847mobile element insertion1nstd206human GRCh38 chr11: 112,344,643-112,344,694 , GRCh37.p13 chr11: 112,215,366-112,215,417 LINC02762
    nsv5511988copy number variation1nstd206human GRCh38 chr11: 112,292,953-112,297,818 , GRCh37.p13 chr11: 112,163,676-112,168,541 LINC02762
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5504448copy number variation1nstd206human GRCh38 chr11: 112,334,657-112,336,477 , GRCh37.p13 chr11: 112,205,380-112,207,200 LOC107984388, LINC02762
    nsv5504002copy number variation1nstd206human GRCh38 chr11: 112,328,233-112,328,359 , GRCh37.p13 chr11: 112,198,956-112,199,082 LINC02762
    nsv5497604copy number variation1nstd206human GRCh38 chr11: 112,331,777-112,331,922 , GRCh37.p13 chr11: 112,202,500-112,202,645 LINC02762
    nsv5495055copy number variation1nstd206human GRCh38 chr11: 112,302,150-112,302,204 , GRCh37.p13 chr11: 112,172,873-112,172,927 LINC02762
    nsv5392531copy number variation2nstd186human GRCh37 chr11: 112,202,500-112,202,645 , GRCh38.p12 chr11: 112,331,777-112,331,922 LINC02762
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373869translocation1nstd200human GRCh38 chr11: 112,297,886-112,297,886 , GRCh38 chr11: 112,292,946-112,292,946 , GRCh37.p13 chr11: 112,163,669-112,163,669 , GRCh37.p13 chr11: 112,168,609-112,168,609 LINC02762
    nsv5337511translocation1nstd200human GRCh37 chr11: 112,163,669-112,163,669 , GRCh37 chr11: 112,168,609-112,168,609 , GRCh38.p12 chr11: 112,292,946-112,292,946 , GRCh38.p12 chr11: 112,297,886-112,297,886 LINC02762
    nsv5333109translocation1nstd200human GRCh37 chr11: 112,163,572-112,163,572 , GRCh37 chr11: 112,163,891-112,163,891 , GRCh38.p12 chr11: 112,292,849-112,292,849 , GRCh38.p12 chr11: 112,293,168-112,293,168 LINC02762
    nsv5311067copy number variation1nstd204human GRCh38.p13 chr11: 112,334,647-112,336,480 , GRCh37.p13 chr11: 112,205,370-112,207,203 LOC107984388, LINC02762
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