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Items: 1 to 20 of 122

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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
    nsv6966603copy number variation1nstd229human GRCh38 chr15: 69,809,540-69,837,168 , GRCh37.p13 chr15: 70,101,879-70,129,507 LINC00593
    nsv6964506copy number variation1nstd229human GRCh38 chr15: 69,840,497-69,881,876 , GRCh37.p13 chr15: 70,132,836-70,174,215 LINC00593
    nsv6958891copy number variation1nstd229human GRCh38 chr15: 69,768,482-69,900,004 , GRCh37.p13 chr15: 70,060,821-70,192,343 LINC00593, GEMIN8P1, 1 more genes
    nsv6958843copy number variation1nstd229human GRCh38 chr15: 69,836,325-69,838,462 , GRCh37.p13 chr15: 70,128,664-70,130,801 LINC00593
    nsv6958168copy number variation1nstd229human GRCh38 chr15: 69,833,432-69,837,457 , GRCh37.p13 chr15: 70,125,771-70,129,796 LINC00593
    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
    nsv6511076copy number variation1nstd223human GRCh38 chr15: 69,840,489-69,881,878 , GRCh37.p13 chr15: 70,132,828-70,174,217 LINC00593
    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
    nsv5974131inversion1nstd209human GRCh38 chr15: 69,829,074-69,834,100 , GRCh37.p13 chr15: 70,121,413-70,126,439 LINC00593
    nsv5928296copy number variation1nstd209human GRCh38 chr15: 69,834,129-69,834,625 , GRCh37.p13 chr15: 70,126,468-70,126,964 LINC00593
    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
    nsv5336100translocation1nstd200human GRCh37 chr15: 70,127,008-70,127,008 , GRCh37 chr15: 70,121,326-70,121,326 , GRCh38.p12 chr15: 69,828,987-69,828,987 , GRCh38.p12 chr15: 69,834,669-69,834,669 LINC00593
    nsv5333867translocation1nstd200human GRCh37 chr15: 70,121,415-70,121,415 , GRCh37 chr15: 70,126,440-70,126,440 , GRCh38.p12 chr15: 69,829,076-69,829,076 , GRCh38.p12 chr15: 69,834,101-69,834,101 LINC00593
    nsv5005544copy number variation1nstd200human GRCh38 chr15: 69,768,481-69,900,005 , GRCh37.p13 chr15: 70,060,820-70,192,344 LINC00593, GEMIN8P1, 1 more genes
    nsv4992203copy number variation1nstd200human GRCh38 chr15: 69,840,064-69,840,216 , GRCh37.p13 chr15: 70,132,403-70,132,555 LINC00593
    nsv4863867copy number variation1nstd200human GRCh37 chr15: 70,060,820-70,192,344 , GRCh38.p12 chr15: 69,768,481-69,900,005 LOC107984788, GEMIN8P1, 1 more genes
    nsv4849986copy number variation1nstd200human GRCh37 chr15: 70,132,403-70,132,555 , GRCh38.p12 chr15: 69,840,064-69,840,216 LINC00593
    nsv4849985copy number variation1nstd200human GRCh37 chr15: 70,126,438-70,127,007 , GRCh38.p12 chr15: 69,834,099-69,834,668 LINC00593
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