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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129410insertion1nstd186human GRCh37 chr15: 49,944,812-49,944,856 , GRCh38.p12 chr15: 49,652,615-49,652,659 DTWD1
    nsv5976925insertion1nstd209human GRCh38 chr15: 49,652,608-49,652,608 , GRCh37.p13 chr15: 49,944,805-49,944,805 DTWD1
    nsv5656985insertion1nstd207human GRCh38 chr15: 49,652,608-49,652,608 , GRCh37.p13 chr15: 49,944,805-49,944,805 DTWD1
    nsv5547841insertion1nstd206human GRCh38 chr15: 49,652,615-49,652,659 , GRCh37.p13 chr15: 49,944,812-49,944,856 DTWD1
    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
    nsv5001728copy number variation1nstd200human GRCh38 chr15: 49,648,326-49,650,129 , GRCh37.p13 chr15: 49,940,523-49,942,326 DTWD1
    nsv5001727copy number variation1nstd200human GRCh38 chr15: 49,642,921-49,645,386 , GRCh37.p13 chr15: 49,935,118-49,937,583 DTWD1
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4866105copy number variation1nstd200human GRCh37 chr15: 49,940,523-49,942,326 , GRCh38.p12 chr15: 49,648,326-49,650,129 DTWD1
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 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
    nsv4644008copy number variation1nstd186human GRCh37 chr15: 49,944,812-49,945,140 , GRCh38.p12 chr15: 49,652,615-49,652,943 DTWD1
    nsv4567823mobile element insertion1nstd166human GRCh37.p13 chr15: 49,924,538-49,924,538 , GRCh38.p12 chr15: 49,632,341-49,632,341 DTWD1
    nsv4530652copy number variation1nstd166human GRCh37.p13 chr15: 49,915,763-49,915,821 , GRCh38.p12 chr15: 49,623,566-49,623,624 DTWD1
    nsv4499963mobile element insertion1nstd166human GRCh37.p13 chr15: 49,922,517-49,922,517 , GRCh38.p12 chr15: 49,630,320-49,630,320 DTWD1
    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
    nsv4455359copy number variation1nstd102humanPathogenic GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199 MIR4716, RPS13P8, 112 more genes
    nsv4245353copy number variation1nstd166human GRCh37.p13 chr15: 49,944,812-49,945,140 , GRCh38.p12 chr15: 49,652,615-49,652,943 DTWD1
    nsv4238010copy number variation1nstd166human GRCh37.p13 chr15: 49,940,523-49,942,326 , GRCh38.p12 chr15: 49,648,326-49,650,129 DTWD1
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