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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713172mobile element insertion1nstd211human GRCh38 chr15: 62,643,440-62,643,440 , GRCh37.p13 chr15: 62,935,639-62,935,639 TLN2, MGC15885
    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
    nsv4991944copy number variation1nstd200human GRCh38 chr15: 62,642,014-62,642,102 , GRCh37.p13 chr15: 62,934,213-62,934,301 MGC15885, TLN2
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4849787copy number variation1nstd200human GRCh37 chr15: 62,934,213-62,934,301 , GRCh38.p12 chr15: 62,642,014-62,642,102 TLN2, MGC15885
    nsv4729260copy number variation1nstd102humanUncertain significance GRCh37 chr15: 62,810,728-63,024,932 , GRCh38.p12 chr15: 62,518,529-62,732,733 MGC15885, TLN2, 1 more genes
    nsv4629761copy number variation1nstd183human GRCh37 chr15: 62,931,493-62,975,055 , GRCh38.p12 chr15: 62,639,294-62,682,856 MGC15885, TLN2, 1 more genes
    nsv4621051copy number variation1nstd183human GRCh37 chr15: 62,830,704-63,435,196 , GRCh38.p12 chr15: 62,538,505-63,142,997 LOC105370855, LOC100287243, 8 more genes
    nsv4244778copy number variation1nstd166human GRCh37.p13 chr15: 62,934,213-62,934,301 , GRCh38.p12 chr15: 62,642,014-62,642,102 MGC15885, TLN2
    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
    nsv3921425copy number variation1nstd102humanPathogenic NCBI36 chr15: 55,647,440-61,098,667 , GRCh37 chr15: 57,860,148-63,311,614 , GRCh38 chr15: 57,567,950-63,019,415 MESTP2, HMGB1P51, 86 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
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 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
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 MIR4513, LOC727751, 1754 more genes
    nsv3911945copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 HDDC3, TRK-CTT16-1, 1622 more genes
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