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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5695903mobile element insertion1nstd211human GRCh38 chr15: 42,188,039-42,188,039 , GRCh37.p13 chr15: 42,480,237-42,480,237 VPS39
    nsv5660685insertion1nstd207human GRCh38 chr15: 42,188,023-42,188,023 , GRCh37.p13 chr15: 42,480,221-42,480,221 VPS39
    nsv5564072sequence alteration1nstd206human GRCh38 chr15: 42,194,628-42,248,498 , GRCh37.p13 chr15: 42,486,826-42,540,696 VPS39, TMEM87A, 2 more genes
    nsv5427160mobile element insertion1nstd206human GRCh38 chr15: 42,188,039-42,188,090 , GRCh37.p13 chr15: 42,480,237-42,480,288 VPS39
    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
    nsv5159326mobile element insertion1nstd203human GRCh38 chr15: 42,188,023-42,188,039 , GRCh37.p13 chr15: 42,480,221-42,480,237 VPS39
    nsv5144615mobile element insertion1nstd203human GRCh38 chr15: 42,188,030-42,188,039 , GRCh37.p13 chr15: 42,480,228-42,480,237 VPS39
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001461copy number variation1nstd200human GRCh38 chr15: 42,206,242-42,206,368 , GRCh37.p13 chr15: 42,498,440-42,498,566 VPS39, VPS39-DT
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4729715copy number variation1nstd102humanLikely benign GRCh37 chr15: 41,869,275-42,484,890 , GRCh38.p12 chr15: 41,577,077-42,192,692 SPTBN5, RNA5SP393, 18 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
    nsv4568457sequence alteration1nstd166human GRCh37.p13 chr15: 42,456,298-42,456,299 , GRCh38.p12 chr15: 42,164,100-42,164,101 VPS39
    nsv4504899mobile element insertion1nstd166human GRCh37.p13 chr15: 42,480,221-42,480,221 , GRCh38.p12 chr15: 42,188,023-42,188,023 VPS39
    nsv4501103mobile element insertion1nstd166human GRCh37.p13 chr15: 42,459,852-42,459,852 , GRCh38.p12 chr15: 42,167,654-42,167,654 VPS39
    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
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