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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933077copy number variation1nstd209human GRCh38 chr15: 41,533,190-41,533,553 , GRCh37.p13 chr15: 41,825,388-41,825,751 RPAP1
    nsv5720774mobile element insertion1nstd211human GRCh38 chr15: 41,515,423-41,515,423 , GRCh37.p13 chr15: 41,807,621-41,807,621 RPAP1
    nsv5511613copy number variation1nstd206human GRCh38 chr15: 41,537,973-41,541,618 , GRCh37.p13 chr15: 41,830,171-41,833,816 RPAP1
    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
    nsv5005307copy number variation1nstd200human GRCh38 chr15: 41,540,451-41,548,072 , GRCh37.p13 chr15: 41,832,649-41,840,270 RPAP1
    nsv5001429copy number variation1nstd200human GRCh38 chr15: 41,532,298-41,532,409 , GRCh37.p13 chr15: 41,824,496-41,824,607 RPAP1
    nsv5001428copy number variation1nstd200human GRCh38 chr15: 41,515,202-41,516,112 , GRCh37.p13 chr15: 41,807,400-41,808,310 RPAP1
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4769462mobile element deletion1nstd200human GRCh37 chr15: 41,814,593-41,814,887 , GRCh38.p12 chr15: 41,522,395-41,522,689 RPAP1
    nsv4541561insertion1nstd166human GRCh37.p13 chr15: 41,809,069-41,809,069 , GRCh38.p12 chr15: 41,516,871-41,516,871 RPAP1
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4247173copy number variation1nstd166human GRCh37.p13 chr15: 41,815,372-41,815,447 , GRCh38.p12 chr15: 41,523,174-41,523,249 RPAP1
    nsv4243549copy number variation1nstd166human GRCh37.p13 chr15: 41,832,671-41,840,216 , GRCh38.p12 chr15: 41,540,473-41,548,018 RPAP1
    nsv4243352copy number variation1nstd166human GRCh37.p13 chr15: 41,805,291-41,820,656 , GRCh38.p12 chr15: 41,513,093-41,528,458 LTK, RPAP1
    nsv4235674copy number variation1nstd166human GRCh37.p13 chr15: 41,816,551-41,821,157 , GRCh38.p12 chr15: 41,524,353-41,528,959 RPAP1
    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
    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
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