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Items: 1 to 20 of 993

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148240copy number variation1nstd102humanPathogenic GRCh38 chrX: 31,782,226-32,088,001 , GRCh37.p13 chrX: 31,800,343-32,106,118 DMD
    nsv7148231copy number variation1nstd102humanPathogenic GRCh38 chrX: 32,536,377-32,771,300 , GRCh37.p13 chrX: 32,554,494-32,789,417 DMD, MIR548F5, 1 more genes
    nsv7148209copy number variation1nstd102humanPathogenic GRCh38 chrX: 31,601,428-31,727,780 , GRCh37.p13 chrX: 31,619,545-31,745,897 DMD
    nsv7148171copy number variation1nstd102humanLikely pathogenic GRCh38 chrX: 31,929,309-31,932,391 , GRCh37.p13 chrX: 31,947,426-31,950,508 DMD
    nsv7148144copy number variation1nstd102humanPathogenic GRCh38 chrX: 32,216,792-33,041,819 , GRCh37.p13 chrX: 32,234,909-33,059,936 MIR548F5, TBCAP1, 2 more genes
    nsv7148140copy number variation1nstd102humanPathogenic GRCh38 chrX: 23,730,430-32,849,918 , GRCh37.p13 chrX: 23,748,547-32,868,035 ARX, LOC107985632, 85 more genes
    nsv7147249insertion1nstd232human GRCh37.p13 chrX: 32,103,719-32,103,719 , GRCh38.p12 chrX: 32,085,602-32,085,602 DMD
    nsv7145233insertion1nstd232human GRCh37.p13 chrX: 31,587,738-31,587,738 , GRCh38.p12 chrX: 31,569,621-31,569,621 DMD
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7137038copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 31,950,355-32,305,635 , GRCh38.p12 chrX: 31,932,238-32,287,518 DMD, NPM1P8, 1 more genes
    nsv7137024copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,366,752-31,854,834 , GRCh38.p12 chrX: 31,348,635-31,836,717 DMD, RNU6-894P
    nsv7137021copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,747,866-31,986,455 , GRCh38.p12 chrX: 31,729,749-31,968,338 DMD
    nsv7137006copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,747,866-32,456,357 , GRCh38.p12 chrX: 31,729,749-32,438,240 NPM1P8, DMD, 1 more genes
    nsv7136972copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,519,960-33,229,674 , GRCh38.p12 chrX: 32,501,843-33,211,557 DMD, MIR3915, 2 more genes
    nsv7099299copy number variation1nstd231human GRCh37 chrX: 31,458,626-31,463,924 , GRCh38.p12 chrX: 31,440,509-31,445,807 DMD
    nsv7099010copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,536,249-32,583,818 , GRCh38.p12 chrX: 32,518,132-32,565,701 DMD
    nsv7099002copy number variation1nstd102humanUncertain significance GRCh37 chrX: 31,137,344-31,366,672 , GRCh38.p12 chrX: 31,119,227-31,348,555 DMD, RNU6-894P
    nsv7098995copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 31,462,745-31,645,789 , GRCh38.p12 chrX: 31,444,628-31,627,672 DMD
    nsv7098982copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 32,235,181-32,583,818 , GRCh38.p12 chrX: 32,217,064-32,565,701 DMD
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