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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125425insertion1nstd186human GRCh37 chr3: 112,304,775-112,304,777 , GRCh38.p12 chr3: 112,585,928-112,585,930 SLC35A5
    nsv5949024insertion1nstd209human GRCh38 chr3: 112,585,929-112,585,929 , GRCh37.p13 chr3: 112,304,776-112,304,776 SLC35A5
    nsv5906297copy number variation1nstd209human GRCh38 chr3: 112,580,706-112,582,668 , GRCh37.p13 chr3: 112,299,553-112,301,515 SLC35A5
    nsv5901928copy number variation1nstd209human GRCh38 chr3: 112,577,281-112,577,363 , GRCh37.p13 chr3: 112,296,128-112,296,210 SLC35A5
    nsv5889528copy number variation1nstd209human GRCh38 chr3: 112,581,325-112,582,668 , GRCh37.p13 chr3: 112,300,172-112,301,515 SLC35A5
    nsv5678527mobile element insertion1nstd211human GRCh38 chr3: 112,577,064-112,577,064 , GRCh37.p13 chr3: 112,295,911-112,295,911 SLC35A5
    nsv5535308insertion1nstd206human GRCh38 chr3: 112,585,928-112,585,930 , GRCh37.p13 chr3: 112,304,775-112,304,777 SLC35A5
    nsv5436315copy number variation1nstd206human GRCh38 chr3: 112,583,486-112,583,587 , GRCh37.p13 chr3: 112,302,333-112,302,434 SLC35A5
    nsv5434958copy number variation1nstd206human GRCh38 chr3: 112,585,023-112,585,081 , GRCh37.p13 chr3: 112,303,870-112,303,928 SLC35A5
    nsv5361854translocation1nstd200human GRCh38 chr18: 13,644,005-13,644,005 , GRCh38 chr3: 112,562,181-112,562,181 , GRCh37.p13 chr18: 13,644,004-13,644,004 , GRCh37.p13 chr3: 112,281,028-112,281,028 LDLRAD4, SLC35A5, 1 more genes
    nsv5346415translocation1nstd200human GRCh38 chr3: 112,581,327-112,581,327 , GRCh38 chr3: 112,582,669-112,582,669 , GRCh37.p13 chr3: 112,301,516-112,301,516 , GRCh37.p13 chr3: 112,300,174-112,300,174 SLC35A5
    nsv5341731translocation1nstd200human GRCh37 chr3: 112,302,434-112,302,434 , GRCh37 chr3: 112,302,333-112,302,333 , GRCh38.p12 chr3: 112,583,587-112,583,587 , GRCh38.p12 chr3: 112,583,486-112,583,486 SLC35A5
    nsv5089711mobile element insertion1nstd203human GRCh38 chr3: 112,566,690-112,566,699 , GRCh37.p13 chr3: 112,285,537-112,285,546 SLC35A5
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919566copy number variation1nstd200human GRCh38 chr3: 112,583,486-112,583,587 , GRCh37.p13 chr3: 112,302,333-112,302,434 SLC35A5
    nsv4914650copy number variation1nstd200human GRCh38 chr3: 112,573,235-112,573,402 , GRCh37.p13 chr3: 112,292,082-112,292,249 SLC35A5
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4728380copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,135,341-115,509,260 , GRCh38.p12 chr3: 112,416,494-115,790,413 SLC35A5, EIF4E2P2, 51 more genes
    nsv4595961copy number variation1nstd183human GRCh37 chr3: 111,977,032-113,013,191 , GRCh38.p12 chr3: 112,258,185-113,294,344 , NEPRO-AS1, 22 more genes
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