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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094481copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,501,523-51,530,610 , GRCh38.p12 chr13: 50,927,387-50,956,474 RNASEH2B
    nsv7094410copy number variation1nstd102humanUncertain significance GRCh37 chr13: 51,484,213-52,602,726 , GRCh38.p12 chr13: 50,910,077-52,028,590 ATP7B, RNA5SP29, 29 more genes
    nsv7094083copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,484,213-51,484,296 , GRCh38.p12 chr13: 50,910,077-50,910,160 RNASEH2B, RNASEH2B-AS1
    nsv7074408inversion1nstd229human GRCh38 chr13: 50,051,000-51,766,155 , GRCh37.p13 chr13: 50,625,136-52,340,291 RPL5P31, INTS6, 31 more genes
    nsv7070621inversion1nstd229human GRCh38 chr13: 49,320,428-51,629,920 , GRCh37.p13 chr13: 49,894,564-52,204,056 MIR3613, RNASEH2B-AS1, 50 more genes
    nsv7065649inversion1nstd229human GRCh38 chr13: 50,056,278-51,765,634 , GRCh37.p13 chr13: 50,630,414-52,339,770 SNRPGP11, DLEU2, 30 more genes
    nsv6957561copy number variation1nstd229human GRCh38 chr13: 49,145,001-51,117,700 , GRCh37.p13 chr13: 49,719,137-51,691,836 TRIM13, EBPL, 40 more genes
    nsv6957139copy number variation1nstd229human GRCh38 chr13: 49,992,901-50,963,900 , GRCh37.p13 chr13: 50,567,037-51,538,036 MIR3613, RNASEH2B-AS1, 15 more genes
    nsv6956501copy number variation1nstd229human GRCh38 chr13: 50,952,049-50,958,110 , GRCh37.p13 chr13: 51,526,185-51,532,246 RNASEH2B
    nsv6955231copy number variation1nstd229human GRCh38 chr13: 49,703,981-51,021,582 , GRCh37.p13 chr13: 50,278,117-51,595,718 KPNA3, RPL18P10, 21 more genes
    nsv6953234copy number variation1nstd229human GRCh38 chr13: 49,610,822-50,909,481 , GRCh37.p13 chr13: 50,184,958-51,483,617 KCNRG, RNA5SP28, 24 more genes
    nsv6952435copy number variation1nstd229human GRCh38 chr13: 48,165,561-51,834,243 , GRCh37.p13 chr13: 48,739,697-52,408,379 LPAR6, RNY4P30, 77 more genes
    nsv6952317copy number variation1nstd229human GRCh38 chr13: 50,935,210-50,940,293 , GRCh37.p13 chr13: 51,509,346-51,514,429 RNASEH2B
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6952110copy number variation1nstd229human GRCh38 chr13: 49,921,931-50,950,891 , GRCh37.p13 chr13: 50,496,067-51,525,027 MIR3613, RNASEH2B-AS1, 16 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6951658copy number variation1nstd229human GRCh38 chr13: 50,968,477-50,968,580 , GRCh37.p13 chr13: 51,542,613-51,542,716 RNASEH2B
    nsv6950725copy number variation1nstd229human GRCh38 chr13: 49,917,693-51,333,587 , GRCh37.p13 chr13: 50,491,829-51,907,723 LOC107984554, ST13P4, 23 more genes
    nsv6950233copy number variation1nstd229human GRCh38 chr13: 49,825,079-50,963,993 , GRCh37.p13 chr13: 50,399,215-51,538,129 RNA5SP28, MIR16-1, 19 more genes
    nsv6948417copy number variation1nstd229human GRCh38 chr13: 50,901,336-50,914,060 , GRCh37.p13 chr13: 51,475,472-51,488,196 RNASEH2B-AS1, RNASEH2B
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