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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963581insertion1nstd209human GRCh38 chr3: 38,555,125-38,555,125 , GRCh37.p13 chr3: 38,596,616-38,596,616 SCN5A
    nsv5952833insertion1nstd209human GRCh38 chr3: 38,584,574-38,584,574 , GRCh37.p13 chr3: 38,626,065-38,626,065 SCN5A
    nsv5894100copy number variation1nstd209human GRCh38 chr3: 38,575,126-38,575,186 , GRCh37.p13 chr3: 38,616,617-38,616,677 SCN5A
    nsv5893353copy number variation1nstd209human GRCh38 chr3: 38,561,816-38,561,878 , GRCh37.p13 chr3: 38,603,307-38,603,369 SCN5A
    nsv5729812mobile element insertion2nstd211human GRCh38 chr3: 38,584,591-38,584,591 , GRCh37.p13 chr3: 38,626,082-38,626,082 SCN5A
    nsv5691163mobile element insertion2nstd211human GRCh38 chr3: 38,597,538-38,597,538 , GRCh37.p13 chr3: 38,639,029-38,639,029 SCN5A
    nsv5673563copy number variation1nstd102humanPathogenic GRCh37 chr3: 38,655,228-38,663,986 , GRCh38.p12 chr3: 38,613,737-38,622,495 SCN5A
    nsv5673484copy number variation1nstd102humanPathogenic GRCh37 chr3: 38,674,520-38,674,804 , GRCh38.p12 chr3: 38,633,029-38,633,313 SCN5A
    nsv5673483copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 38,591,792-38,593,069 , GRCh38.p12 chr3: 38,550,301-38,551,578 SCN5A
    nsv5609939insertion1nstd207human GRCh38 chr3: 38,584,574-38,584,574 , GRCh37.p13 chr3: 38,626,065-38,626,065 SCN5A
    nsv5570556copy number variation1nstd207human GRCh38 chr3: 38,561,816-38,561,878 , GRCh37.p13 chr3: 38,603,307-38,603,369 SCN5A
    nsv5562209sequence alteration1nstd206human GRCh38 chr3: 38,502,175-38,676,379 , GRCh37.p13 chr3: 38,543,666-38,717,870 SCN5A, EXOG, 2 more genes
    nsv5557500mobile element insertion1nstd206human GRCh38 chr3: 38,584,591-38,584,642 , GRCh37.p13 chr3: 38,626,082-38,626,133 SCN5A
    nsv5440965copy number variation1nstd206human GRCh38 chr3: 38,575,128-38,575,187 , GRCh37.p13 chr3: 38,616,619-38,616,678 SCN5A
    nsv5410098mobile element insertion1nstd206human GRCh38 chr3: 38,597,538-38,597,589 , GRCh37.p13 chr3: 38,639,029-38,639,080 SCN5A
    nsv5381596copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,616,778-38,620,996 , GRCh38.p12 chr3: 38,575,287-38,579,505 SCN5A
    nsv5381496copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,591,802-38,991,863 , GRCh38.p12 chr3: 38,550,311-38,950,372 SCN11A, SCN5A, 3 more genes
    nsv5339085translocation1nstd200human GRCh37 chr3: 38,616,678-38,616,678 , GRCh37 chr3: 38,616,619-38,616,619 , GRCh38.p12 chr3: 38,575,128-38,575,128 , GRCh38.p12 chr3: 38,575,187-38,575,187 SCN5A
    nsv5311142copy number variation1nstd204human GRCh37.p13 chr3: 38,551,117-38,955,783 , GRCh38.p13 chr3: 38,509,626-38,914,292 SCN5A, SCN10A, 6 more genes
    nsv5217069copy number variation1nstd204human GRCh38.p13 chr3: 38,553,752-38,554,851 , GRCh37.p13 chr3: 38,595,243-38,596,342 SCN5A
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