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Items: 1 to 20 of 473

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094409copy number variation1nstd102humanUncertain significance GRCh37 chr13: 50,129,631-50,129,829 , GRCh38.p12 chr13: 49,555,495-49,555,693 RCBTB1
    nsv7094082copy number variation1nstd102humanUncertain significance GRCh37 chr13: 50,140,734-50,141,415 , GRCh38.p12 chr13: 49,566,598-49,567,279 RCBTB1
    nsv7094081copy number variation1nstd102humanUncertain significance GRCh37 chr13: 50,123,574-50,141,415 , GRCh38.p12 chr13: 49,549,438-49,567,279 RCBTB1
    nsv7094080copy number variation1nstd102humanUncertain significance GRCh37 chr13: 50,114,992-50,115,162 , GRCh38.p12 chr13: 49,540,856-49,541,026 RCBTB1
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 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
    nsv7062591inversion1nstd229human GRCh38 chr13: 49,445,029-50,859,553 , GRCh37.p13 chr13: 50,019,165-51,433,689 PHF11, RPL34P26, 28 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
    nsv6955785copy number variation1nstd229human GRCh38 chr13: 49,570,601-49,574,000 , GRCh37.p13 chr13: 50,144,737-50,148,136 RCBTB1
    nsv6954991copy number variation1nstd229human GRCh38 chr13: 49,578,794-49,584,777 , GRCh37.p13 chr13: 50,152,930-50,158,913 RCBTB1
    nsv6952872copy number variation1nstd229human GRCh38 chr13: 49,496,001-49,792,600 , GRCh37.p13 chr13: 50,070,137-50,366,736 PHF11, RCBTB1, 6 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
    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
    nsv6952184copy number variation1nstd229human GRCh38 chr13: 49,403,601-50,069,700 , GRCh37.p13 chr13: 49,977,737-50,643,836 CTAGE10P, RNY4P9, 19 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
    nsv6951616copy number variation1nstd229human GRCh38 chr13: 49,557,471-49,615,799 , GRCh37.p13 chr13: 50,131,607-50,189,935 RCBTB1, LOC105370204
    nsv6951514copy number variation1nstd229human GRCh38 chr13: 49,452,312-49,619,991 , GRCh37.p13 chr13: 50,026,448-50,194,127 SETDB2, PHF11, 4 more genes
    nsv6949479copy number variation1nstd229human GRCh38 chr13: 49,493,001-49,606,900 , GRCh37.p13 chr13: 50,067,137-50,181,036 SETDB2, RCBTB1, 2 more genes
    nsv6947937copy number variation1nstd229human GRCh38 chr13: 48,313,660-50,916,452 , GRCh37.p13 chr13: 48,887,796-51,490,588 MIR16-1, PCNPP5, 51 more genes
    nsv6947585copy number variation1nstd229human GRCh38 chr13: 48,556,959-51,460,180 , GRCh37.p13 chr13: 49,131,095-52,034,316 RNY4P9, GUCY1B2, 57 more genes
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