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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073147inversion1nstd229human GRCh38 chr15: 43,268,512-43,276,127 , GRCh37.p13 chr15: 43,560,710-43,568,325 ATP5PDP1, TGM7
    nsv7066408inversion1nstd229human GRCh38 chr15: 43,278,449-43,283,039 , GRCh37.p13 chr15: 43,570,647-43,575,237 TGM7
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6967231copy number variation1nstd229human GRCh38 chr15: 43,282,345-43,292,267 , GRCh37.p13 chr15: 43,574,543-43,584,465 TGM7
    nsv6966689copy number variation1nstd229human GRCh38 chr15: 43,124,367-43,284,900 , GRCh37.p13 chr15: 43,416,565-43,577,098 EPB42, TGM5, 6 more genes
    nsv6963399copy number variation1nstd229human GRCh38 chr15: 43,283,411-43,292,065 , GRCh37.p13 chr15: 43,575,609-43,584,263 TGM7
    nsv6963230copy number variation1nstd229human GRCh38 chr15: 43,278,815-43,334,747 , GRCh37.p13 chr15: 43,571,013-43,626,945 ADAL, LCMT2, 1 more genes
    nsv6511435copy number variation1nstd223human GRCh38 chr15: 43,282,345-43,292,265 , GRCh37.p13 chr15: 43,574,543-43,584,463 TGM7
    nsv6501688copy number variation1nstd223human GRCh38 chr15: 43,295,452-43,297,188 , GRCh37.p13 chr15: 43,587,650-43,589,386 TGM7
    nsv6496110copy number variation1nstd223human GRCh38 chr15: 43,175,921-43,650,339 , GRCh37.p13 chr15: 43,468,119-43,942,537 ADAL, EPB42, 19 more genes
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv5509528copy number variation1nstd206human GRCh38 chr15: 43,282,345-43,292,265 , GRCh37.p13 chr15: 43,574,543-43,584,463 TGM7
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357865translocation1nstd200human GRCh38 chr15: 43,282,345-43,282,345 , GRCh38 chr15: 43,292,265-43,292,265 , GRCh37.p13 chr15: 43,574,543-43,574,543 , GRCh37.p13 chr15: 43,584,463-43,584,463 TGM7
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001504copy number variation1nstd200human GRCh38 chr15: 43,295,446-43,297,198 , GRCh37.p13 chr15: 43,587,644-43,589,396 TGM7
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4865947copy number variation1nstd200human GRCh37 chr15: 43,587,635-43,589,408 , GRCh38.p12 chr15: 43,295,437-43,297,210 TGM7
    nsv4741577copy number variation1nstd199human GRCh37 chr15: 43,585,934-43,586,001 , GRCh38.p12 chr15: 43,293,736-43,293,803 TGM7
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