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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7064235inversion1nstd229human GRCh38 chr15: 68,177,132-69,135,262 , GRCh37.p13 chr15: 68,469,470-69,427,601 CORO2B, LOC105370873, 16 more genes
    nsv7063928inversion1nstd229human GRCh38 chr15: 69,083,281-69,088,537 , GRCh37.p13 chr15: 69,375,621-69,380,877 EWSAT1
    nsv7063557inversion1nstd229human GRCh38 chr15: 68,148,341-69,105,455 , GRCh37.p13 chr15: 68,440,679-69,397,795 ITGA11, MIR4312, 16 more genes
    nsv7058734inversion1nstd229human GRCh38 chr15: 68,148,356-69,105,454 , GRCh37.p13 chr15: 68,440,694-69,397,794 LOC105370873, CORO2B, 16 more genes
    nsv6967949copy number variation1nstd229human GRCh38 chr15: 68,997,019-69,110,170 , GRCh37.p13 chr15: 69,289,358-69,402,510 NOX5, LOC100422194, 1 more genes
    nsv6966552copy number variation1nstd229human GRCh38 chr15: 69,079,345-69,080,191 , GRCh37.p13 chr15: 69,371,685-69,372,531 EWSAT1
    nsv6963783copy number variation1nstd229human GRCh38 chr15: 69,079,022-69,092,997 , GRCh37.p13 chr15: 69,371,362-69,385,337 EWSAT1
    nsv6637906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 68,807,665-70,981,473 , GRCh38.p12 chr15: 68,515,326-70,689,134 UACA, RPLP1, 36 more genes
    nsv6496080copy number variation1nstd223human GRCh38 chr15: 69,065,055-69,110,341 , GRCh37.p13 chr15: 69,357,395-69,402,681 EWSAT1
    nsv6495966copy number variation1nstd223human GRCh38 chr15: 69,093,740-69,096,802 , GRCh37.p13 chr15: 69,386,080-69,389,142 EWSAT1
    nsv6132961copy number variation1nstd213human GRCh37 chr15: 69,080,000-73,430,001 , GRCh38.p12 chr15: 68,787,661-73,137,660 BBS4, MYO9A, 84 more genes
    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
    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
    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
    nsv4248839copy number variation1nstd166human GRCh37.p13 chr15: 69,380,771-69,381,245 , GRCh38.p12 chr15: 69,088,431-69,088,905 EWSAT1
    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
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