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Items: 1 to 20 of 788

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7141223copy number variation1nstd232human GRCh37.p13 chr5: 10,640,126-10,640,245 , GRCh38.p12 chr5: 10,640,014-10,640,133 ANKRD33B
    nsv7098841copy number variation1nstd102humanPathogenic GRCh37 chr5: 10,149,255-18,180,300 , GRCh38.p12 chr5: 10,149,143-18,180,191 RN7SKP133, TAF11L1, 102 more genes
    nsv7040120inversion1nstd229human GRCh38 chr5: 10,579,130-10,579,178 , GRCh37.p13 chr5: 10,579,242-10,579,290 ANKRD33B
    nsv6777839copy number variation1nstd229human GRCh38 chr5: 10,586,325-10,590,469 , GRCh37.p13 chr5: 10,586,437-10,590,581 ANKRD33B
    nsv6776887copy number variation1nstd229human GRCh38 chr5: 10,656,708-10,661,110 , GRCh37.p13 chr5: 10,656,820-10,661,222 ANKRD33B
    nsv6776871copy number variation1nstd229human GRCh38 chr5: 10,634,101-10,637,500 , GRCh37.p13 chr5: 10,634,213-10,637,612 ANKRD33B
    nsv6776699copy number variation1nstd229human GRCh38 chr5: 10,568,061-10,568,243 , GRCh37.p13 chr5: 10,568,173-10,568,355 ANKRD33B
    nsv6775248copy number variation1nstd229human GRCh38 chr5: 10,532,001-10,793,300 , GRCh37.p13 chr5: 10,532,113-10,793,412 DAP-DT, CTD-2154B17.1, 3 more genes
    nsv6772316copy number variation1nstd229human GRCh38 chr5: 10,603,406-10,608,435 , GRCh37.p13 chr5: 10,603,518-10,608,547 ANKRD33B
    nsv6766975copy number variation1nstd229human GRCh38 chr5: 10,643,275-10,643,308 , GRCh37.p13 chr5: 10,643,387-10,643,420 ANKRD33B
    nsv6766002copy number variation1nstd229human GRCh38 chr5: 10,203,601-10,797,600 , GRCh37.p13 chr5: 10,203,713-10,797,712 LOC645763, DAP, 16 more genes
    nsv6759132copy number variation1nstd229human GRCh38 chr5: 10,618,914-10,620,338 , GRCh37.p13 chr5: 10,619,026-10,620,450 ANKRD33B
    nsv6758739copy number variation1nstd229human GRCh38 chr5: 10,600,501-10,620,300 , GRCh37.p13 chr5: 10,600,613-10,620,412 ANKRD33B
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6630206copy number variation1nstd224human GRCh37 chr5: 10,578,303-11,233,371 , GRCh38.p12 chr5: 10,578,191-11,233,259 CTNND2, DAP, 6 more genes
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