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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967813insertion1nstd209human GRCh38 chr15: 48,159,005-48,159,005 , GRCh37.p13 chr15: 48,451,202-48,451,202 MYEF2
    nsv5944228copy number variation1nstd209human GRCh38 chr15: 48,152,993-48,153,043 , GRCh37.p13 chr15: 48,445,190-48,445,240 MYEF2
    nsv5710909mobile element insertion1nstd211human GRCh38 chr15: 48,171,449-48,171,449 , GRCh37.p13 chr15: 48,463,646-48,463,646 MYEF2
    nsv5708294mobile element insertion2nstd211human GRCh38 chr15: 48,159,019-48,159,019 , GRCh37.p13 chr15: 48,451,216-48,451,216 MYEF2
    nsv5600301copy number variation1nstd207human GRCh38 chr15: 48,152,993-48,153,043 , GRCh37.p13 chr15: 48,445,190-48,445,240 MYEF2
    nsv5419241mobile element insertion1nstd206human GRCh38 chr15: 48,159,019-48,159,070 , GRCh37.p13 chr15: 48,451,216-48,451,267 MYEF2
    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
    nsv5149179mobile element insertion1nstd203human GRCh38 chr15: 48,159,005-48,159,019 , GRCh37.p13 chr15: 48,451,202-48,451,216 MYEF2
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001681copy number variation1nstd200human GRCh38 chr15: 47,881,221-48,441,463 , GRCh37.p13 chr15: 48,173,418-48,733,660 , 14 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
    nsv4866080copy number variation1nstd200human GRCh37 chr15: 48,437,976-48,438,630 , GRCh38.p12 chr15: 48,145,779-48,146,433 MYEF2
    nsv4866068copy number variation1nstd200human GRCh37 chr15: 48,173,418-48,733,660 , GRCh38.p12 chr15: 47,881,221-48,441,463 , FBN1, 14 more genes
    nsv4682714copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,426,485-48,936,976 , GRCh38.p12 chr15: 48,134,288-48,644,779 DUT, FBN1, 7 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
    nsv4640958copy number variation1nstd186human GRCh37 chr15: 48,445,191-48,445,241 , GRCh38.p12 chr15: 48,152,994-48,153,044 MYEF2
    nsv4624978copy number variation1nstd183human GRCh37 chr15: 48,458,082-48,458,362 , GRCh38.p12 chr15: 48,165,885-48,166,165 MYEF2
    nsv4510568mobile element insertion1nstd166human GRCh37.p13 chr15: 48,451,202-48,451,202 , GRCh38.p12 chr15: 48,159,005-48,159,005 MYEF2
    nsv4501037mobile element insertion1nstd166human GRCh37.p13 chr15: 48,456,155-48,456,155 , GRCh38.p12 chr15: 48,163,958-48,163,958 MYEF2
    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
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