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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5261752copy number variation1nstd204human GRCh38.p13 chr15: 68,819,401-68,984,500 , GRCh37.p13 chr15: 69,111,740-69,276,839 NOX5, ANP32A, 2 more genes
    nsv5155284mobile element insertion1nstd203human GRCh38 chr15: 68,937,134-68,937,150 , GRCh37.p13 chr15: 69,229,473-69,229,489 NOX5, SPESP1
    nsv5005537copy number variation1nstd200human GRCh38 chr15: 68,782,548-69,149,608 , GRCh37.p13 chr15: 69,074,887-69,441,947 NOX5, EWSAT1, 6 more genes
    nsv4511932mobile element insertion1nstd166human GRCh37.p13 chr15: 69,229,473-69,229,473 , GRCh38.p12 chr15: 68,937,134-68,937,134 NOX5, SPESP1
    nsv4456268copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,369,118-70,481,307 , GRCh38.p12 chr15: 67,076,780-70,188,968 ANP32A-IT1, CARS1P1, 48 more genes
    nsv4372845copy number variation1nstd173human GRCh37 chr15: 69,080,386-69,242,927 , GRCh38.p12 chr15: 68,788,047-68,950,588 NOX5, LOC390600, 4 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
    nsv3920633copy number variation1nstd102humanPathogenic GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678 NEO1, LOC390600, 95 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
    nsv3918098copy number variation1nstd102humanUncertain significance NCBI36 chr15: 66,931,182-67,077,978 , GRCh37.p13 chr15: 69,144,128-69,290,924 , GRCh38.p12 chr15: 68,851,789-68,998,585 SPESP1, NOX5
    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
    nsv3914011copy number variation1nstd102humanPathogenic NCBI36 chr15: 65,273,973-67,165,679 , GRCh37 chr15: 67,486,919-69,378,625 , GRCh38 chr15: 67,194,581-69,086,285 LOC105370871, IQCH-AS1, 29 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
    nsv3905308copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 59,297,293-102,480,888 , GRCh38.p12 chr15: 59,005,094-101,940,685 ACAN, ALDH1A3, 861 more genes
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