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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098681copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 99,551,275-101,097,764 , GRCh38.p12 chrX: 100,296,277-101,842,792 TMEM35A, TNMD, 43 more genes
    nsv7090455copy number variation1nstd229human GRCh38 chrX: 100,946,109-100,967,646 , GRCh37.p13 chrX: 100,201,098-100,222,635 ARL13A, CSGALNACT2P1, 1 more genes
    nsv7090454copy number variation1nstd229human GRCh38 chrX: 100,935,032-100,941,817 , GRCh37.p13 chrX: 100,190,021-100,196,806 XKRX
    nsv7090453copy number variation1nstd229human GRCh38 chrX: 100,920,978-100,989,230 , GRCh37.p13 chrX: 100,175,967-100,244,219 CSGALNACT2P1, TRMT2B, 2 more genes
    nsv7090452copy number variation1nstd229human GRCh38 chrX: 100,917,749-100,917,847 , GRCh37.p13 chrX: 100,172,738-100,172,836 XKRX
    nsv7090451copy number variation1nstd229human GRCh38 chrX: 100,908,674-100,918,443 , GRCh37.p13 chrX: 100,163,663-100,173,432 XKRX, NSA2P3
    nsv7090450copy number variation1nstd229human GRCh38 chrX: 100,908,673-100,912,873 , GRCh37.p13 chrX: 100,163,662-100,167,862 NSA2P3, XKRX
    nsv7090449copy number variation1nstd229human GRCh38 chrX: 100,908,101-100,918,600 , GRCh37.p13 chrX: 100,163,090-100,173,589 XKRX, NSA2P3
    nsv7090448copy number variation1nstd229human GRCh38 chrX: 100,901,930-100,911,158 , GRCh37.p13 chrX: 100,156,919-100,166,147 NSA2P3, XKRX
    nsv7090447copy number variation1nstd229human GRCh38 chrX: 100,901,698-100,901,993 , GRCh37.p13 chrX: 100,156,687-100,156,982 XKRX
    nsv7090446copy number variation1nstd229human GRCh38 chrX: 100,897,222-100,927,177 , GRCh37.p13 chrX: 100,152,211-100,182,166 NSA2P3, XKRX
    nsv7090445copy number variation1nstd229human GRCh38 chrX: 100,891,601-100,894,000 , GRCh37.p13 chrX: 100,146,590-100,148,989 XKRX
    nsv7090444copy number variation1nstd229human GRCh38 chrX: 100,889,786-100,889,921 , GRCh37.p13 chrX: 100,144,775-100,144,910 XKRX
    nsv7090439copy number variation1nstd229human GRCh38 chrX: 100,846,542-100,895,877 , GRCh37.p13 chrX: 100,101,531-100,150,866 NOX1, HNRNPA1P27, 2 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6636525copy number variation1nstd102humanUncertain significance GRCh37 chrX: 100,118,775-100,510,437 , GRCh38.p12 chrX: 100,863,786-101,255,448 HNRNPA1P27, TMEM35A, 9 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634295copy number variation1nstd224human GRCh37 chrX: 99,957,026-100,400,154 , GRCh38.p12 chrX: 100,702,030-101,145,165 CENPI, TRMT2B, 12 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
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