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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5665169inversion1nstd207human GRCh38 chr15: 40,291,941-40,299,299 , GRCh37.p13 chr15: 40,584,142-40,591,500 PLCB2
    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
    nsv5190703mobile element insertion1nstd203human GRCh38 chr15: 40,301,230-40,301,235 , GRCh37.p13 chr15: 40,593,431-40,593,436 PLCB2
    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
    nsv4729095copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,464,942-41,196,807 , GRCh38.p12 chr15: 40,172,741-40,904,609 SPINT1-AS1, KNSTRN, 37 more genes
    nsv4727860copy number variation1nstd197human GRCh38.p12 chr15: 40,291,019-40,291,650 , GRCh37 chr15: 40,583,220-40,583,851 PLCB2
    nsv4623684copy number variation1nstd183human GRCh37 chr15: 40,589,464-40,590,384 , GRCh38.p12 chr15: 40,297,263-40,298,183 PLCB2
    nsv4619342copy number variation1nstd183human GRCh37 chr15: 40,589,502-40,590,372 , GRCh38.p12 chr15: 40,297,301-40,298,171 PLCB2
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4251924copy number variation1nstd166human GRCh37.p13 chr15: 40,575,341-40,575,697 , GRCh38.p12 chr15: 40,283,140-40,283,496 PLCB2
    nsv4248638copy number variation1nstd166human GRCh37.p13 chr15: 40,588,751-40,588,821 , GRCh38.p12 chr15: 40,296,550-40,296,620 PLCB2
    nsv4235924copy number variation1nstd166human GRCh37.p13 chr15: 40,600,228-40,600,322 , GRCh38.p12 chr15: 40,308,027-40,308,121 LOC112268152, PLCB2
    nsv4235736copy number variation1nstd166human GRCh37.p13 chr15: 40,595,497-40,597,812 , GRCh38.p12 chr15: 40,303,296-40,305,611 PLCB2
    nsv3923477copy number variation1nstd102humanUncertain significance NCBI36 chr15: 37,790,428-38,374,084 , GRCh37 chr15: 40,003,136-40,586,792 , GRCh38 chr15: 39,710,935-40,294,591 BMF, MTND5P37, 17 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
    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
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