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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075791inversion1nstd229human GRCh38 chr15: 42,194,627-42,248,499 , GRCh37.p13 chr15: 42,486,825-42,540,697 TMEM87A, MIR627, 2 more genes
    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
    nsv6964218copy number variation1nstd229human GRCh38 chr15: 41,758,370-42,299,821 , GRCh37.p13 chr15: 42,050,568-42,592,019 LOC105370793, RNA5SP393, 19 more genes
    nsv6587307inversion1nstd223human GRCh38 chr15: 42,196,023-42,247,614 , GRCh37.p13 chr15: 42,488,221-42,539,812 VPS39, TMEM87A, 2 more genes
    nsv6132952copy number variation1nstd213human GRCh37 chr15: 42,480,000-43,110,001 , GRCh38.p12 chr15: 42,187,802-42,817,803 GANC, VPS39, 17 more genes
    nsv5564072sequence alteration1nstd206human GRCh38 chr15: 42,194,628-42,248,498 , GRCh37.p13 chr15: 42,486,826-42,540,696 VPS39, TMEM87A, 2 more genes
    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
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4621732copy number variation1nstd183human GRCh37 chr15: 42,156,134-42,638,503 , GRCh38.p12 chr15: 41,863,936-42,346,305 BNIP3P5, PLA2G4D, 14 more genes
    nsv4241942copy number variation1nstd166human GRCh37.p13 chr15: 42,491,291-42,559,476 , GRCh38.p12 chr15: 42,199,093-42,267,278 VPS39-DT, VPS39, 2 more genes
    nsv3924352copy number variation1nstd102humanUncertain significance GRCh38 chr15: 41,697,762-42,489,559 , NCBI36 chr15: 39,777,252-40,569,049 , GRCh37 chr15: 41,989,960-42,781,757 CAPN3, TMEM87A, 25 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919796copy number variation1nstd102humanUncertain significance GRCh37 chr15: 42,157,320-42,621,682 , NCBI36 chr15: 39,944,612-40,408,974 , GRCh38 chr15: 41,865,122-42,329,484 GANC, PLA2G4D, 14 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
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