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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074939inversion1nstd229human GRCh38 chr13: 56,931,806-57,950,142 , GRCh37.p13 chr13: 57,505,940-58,524,276 PRR20D, PRR20A, 11 more genes
    nsv7071638inversion1nstd229human GRCh38 chr13: 55,583,879-63,209,085 , GRCh37.p13 chr13: 56,158,014-63,783,218 MIR3169, PCDH20, 66 more genes
    nsv7070512inversion1nstd229human GRCh38 chr13: 55,145,352-59,139,429 , GRCh37.p13 chr13: 55,719,487-59,713,563 RNY4P29, RPL31P53, 29 more genes
    nsv7059364inversion1nstd229human GRCh38 chr13: 55,085,916-59,699,318 , GRCh37.p13 chr13: 55,660,051-60,273,452 LOC107984625, RN7SKP6, 35 more genes
    nsv6950525copy number variation1nstd229human GRCh38 chr13: 56,224,391-57,241,216 , GRCh37.p13 chr13: 56,798,525-57,815,350 MTCO2P3, RN7SKP6, 8 more genes
    nsv6637880copy number variation1nstd102humanUncertain significance GRCh37 chr13: 56,897,737-64,074,025 , GRCh38.p12 chr13: 56,323,603-63,499,892 DIAPH3-AS2, LOC107984625, 64 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622394copy number variation1nstd224human GRCh37 chr13: 57,711,035-57,874,418 , GRCh38.p12 chr13: 57,136,901-57,300,284 PRR20A, PRR20B, 6 more genes
    nsv6622162copy number variation21nstd224human GRCh37 chr13: 57,711,035-57,822,208 , GRCh38.p12 chr13: 57,136,901-57,248,074 PRR20A, PRR20B, 6 more genes
    nsv6622161copy number variation1nstd224human GRCh37 chr13: 57,539,324-57,903,238 , GRCh38.p12 chr13: 56,965,190-57,329,104 PRR20A, PRR20B, 7 more genes
    nsv6622069copy number variation15nstd224human GRCh37 chr13: 57,708,749-57,820,895 , GRCh38.p12 chr13: 57,134,615-57,246,761 PRR20A, PRR20B, 6 more genes
    nsv6621940copy number variation1nstd224human GRCh37 chr13: 57,635,747-57,818,743 , GRCh38.p12 chr13: 57,061,613-57,244,609 PRR20A, PRR20B, 6 more genes
    nsv6495465copy number variation1nstd223human GRCh38 chr13: 56,956,473-57,337,350 , GRCh37.p13 chr13: 57,530,607-57,911,484 PRR20C, PRR20E, 7 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6291713copy number variation1nstd102humanUncertain significance GRCh37 chr13: 56,995,788-59,674,029 , GRCh38.p12 chr13: 56,421,654-59,099,895 POLR3KP1, PRR20C, 25 more genes
    nsv6291542copy number variation1nstd102humanLikely benign GRCh37 chr13: 55,786,204-58,050,846 , GRCh38.p12 chr13: 55,212,069-57,476,712 PRR20E, HNF4GP1, 13 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6290319copy number variation1nstd102humanPathogenic GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079 CNMD, CPB2-AS1, 241 more genes
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