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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939599copy number variation1nstd209human GRCh38 chr15: 56,780,964-56,943,658 , GRCh37.p13 chr15: 57,073,162-57,235,856 LOC645877, LINC03065, 2 more genes
    nsv5933366copy number variation1nstd209human GRCh38 chr15: 56,918,904-56,919,888 , GRCh37.p13 chr15: 57,211,102-57,212,086 TCF12-DT, TCF12
    nsv5862917copy number variation1nstd209human GRCh38 chr15: 56,900,857-56,909,545 , GRCh37.p13 chr15: 57,193,055-57,201,743 TCF12-DT
    nsv5858538copy number variation1nstd209human GRCh38 chr15: 56,880,549-56,887,831 , GRCh37.p13 chr15: 57,172,747-57,180,029 TCF12-DT, LINC03065
    nsv5695030mobile element insertion1nstd211human GRCh38 chr15: 56,893,142-56,893,142 , GRCh37.p13 chr15: 57,185,340-57,185,340 TCF12-DT
    nsv5422049mobile element insertion1nstd206human GRCh38 chr15: 56,893,142-56,893,193 , GRCh37.p13 chr15: 57,185,340-57,185,391 TCF12-DT
    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
    nsv5005451copy number variation1nstd200human GRCh38 chr15: 56,838,307-56,921,339 , GRCh37.p13 chr15: 57,130,505-57,213,537 LOC645877, TCF12, 2 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
    nsv4529646copy number variation1nstd166human GRCh37.p13 chr15: 57,211,105-57,212,087 , GRCh38.p12 chr15: 56,918,907-56,919,889 TCF12, TCF12-DT
    nsv4513707mobile element insertion1nstd166human GRCh37.p13 chr15: 57,187,741-57,187,741 , GRCh38.p12 chr15: 56,895,543-56,895,543 TCF12-DT
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4391337copy number variation1nstd171human GRCh37 chr15: 57,176,675-57,176,807 , GRCh38.p12 chr15: 56,884,477-56,884,609 TCF12-DT, LINC03065
    nsv4248868copy number variation1nstd166human GRCh37.p13 chr15: 57,173,334-57,177,011 , GRCh38.p12 chr15: 56,881,136-56,884,813 LINC03065, TCF12-DT
    nsv4235477copy number variation1nstd166human GRCh37.p13 chr15: 57,204,448-57,209,163 , GRCh38.p12 chr15: 56,912,250-56,916,965 TCF12, TCF12-DT
    nsv3939765insertion1nstd167human GRCh37 chr15: 57,194,327-57,194,327 , GRCh38.p12 chr15: 56,902,129-56,902,129 TCF12-DT
    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
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