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Items: 1 to 20 of 966

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115326copy number variation1nstd186human GRCh37 chr8: 7,151,722-7,255,972 , GRCh38.p12 chr8: 7,294,200-7,398,450 USP17L1, LOC402329, 6 more genes
    nsv5862874copy number variation2nstd209human GRCh38 chr8: 7,295,595-7,296,794 , GRCh37.p13 chr8: 7,153,117-7,154,316 FAM90A20, FAM66B
    nsv5862528copy number variation2nstd209human GRCh38 chr8: 7,343,447-7,348,616 , GRCh37.p13 chr8: 7,200,969-7,206,138 LOC402329, FAM66B
    nsv5861271copy number variation2nstd209human GRCh38 chr8: 7,295,794-7,297,494 , GRCh37.p13 chr8: 7,153,316-7,155,016 FAM90A20, FAM66B
    nsv5853111copy number variation3nstd209human GRCh38 chr8: 7,353,992-7,370,455 , GRCh37.p13 chr8: 7,211,514-7,227,977 ZNF705G, FAM66B
    nsv5850695copy number variation2nstd209human GRCh38 chr8: 7,295,795-7,298,111 , GRCh37.p13 chr8: 7,153,317-7,155,633 FAM66B, FAM90A20
    nsv5849167copy number variation2nstd209human GRCh38 chr8: 7,343,446-7,347,626 , GRCh37.p13 chr8: 7,200,968-7,205,148 LOC402329, FAM66B
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5575646copy number variation1nstd207human GRCh38 chr8: 7,283,531-7,298,772 , GRCh37.p13 chr8: 7,141,053-7,156,294 FAM90A13, FAM90A5, 2 more genes
    nsv5574447copy number variation1nstd207human GRCh38 chr8: 7,282,485-7,748,748 , GRCh37.p13 chr8: 7,140,007-7,606,270 , DEFB104B, 35 more genes
    nsv5490620copy number variation1nstd206human GRCh38 chr8: 6,692,000-7,616,000 , GRCh37.p13 chr8: 6,549,521-7,473,522 LOC100422495, DEFT1P, 64 more genes
    nsv5485041copy number variation1nstd206human GRCh38 chr8: 7,318,223-7,318,348 , GRCh37.p13 chr8: 7,175,745-7,175,870 DEFB109B, FAM66B
    nsv5477050copy number variation1nstd206human GRCh38 chr8: 7,322,860-7,323,221 , GRCh37.p13 chr8: 7,180,382-7,180,743 FAM66B
    nsv5474475copy number variation1nstd206human GRCh38 chr8: 7,346,676-7,346,786 , GRCh37.p13 chr8: 7,204,198-7,204,308 FAM66B
    nsv5431150copy number variation1nstd206human GRCh38 chr8: 7,294,200-7,398,450 , GRCh37.p13 chr8: 7,151,722-7,255,972 USP17L1, LOC402329, 6 more genes
    nsv5260077copy number variation1nstd204human GRCh37.p13 chr8: 7,206,323-7,308,722 , GRCh38.p13 chr8: 7,348,801-7,451,200 HSPD1P3, SPAG11B, 5 more genes
    nsv5258123copy number variation1nstd204human GRCh38.p13 chr8: 7,353,601-7,357,175 , GRCh37.p13 chr8: 7,211,123-7,214,697 ZNF705G, FAM66B
    nsv5257569copy number variation1nstd204human GRCh38.p13 chr8: 7,348,253-7,357,779 , GRCh37.p13 chr8: 7,205,775-7,215,301 FAM66B, ZNF705G
    nsv5256916copy number variation1nstd204human GRCh38.p13 chr8: 7,353,801-7,370,600 , GRCh37.p13 chr8: 7,211,323-7,228,122 FAM66B, ZNF705G
    nsv5256349copy number variation1nstd204human GRCh38.p13 chr8: 7,325,201-7,326,100 , GRCh37.p13 chr8: 7,182,723-7,183,622 FAM66B
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