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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093994copy number variation1nstd102humanPathogenic GRCh37 chr13: 24,293,859-26,594,123 , GRCh38.p12 chr13: 23,719,720-26,019,985 IRX1P1, MTCO3P2, 54 more genes
    nsv7077553inversion1nstd229human GRCh38 chr13: 22,904,574-24,978,653 , GRCh37.p13 chr13: 23,478,713-25,552,791 SPATA13, TPTE2P6, 52 more genes
    nsv7073256inversion1nstd229human GRCh38 chr13: 19,714,497-24,851,015 , GRCh37.p13 chr13: 20,288,637-25,425,153 SPATA13, IFT88, 114 more genes
    nsv7071034inversion1nstd229human GRCh38 chr13: 19,239,514-24,381,508 , GRCh37.p13 chr13: 19,813,654-24,955,646 BASP1P1, ZMYM5, 111 more genes
    nsv7068132inversion1nstd229human GRCh38 chr13: 23,065,120-25,014,021 , GRCh37.p13 chr13: 23,639,259-25,588,159 TATDN2P3, LOC105370113, 49 more genes
    nsv7067925inversion1nstd229human GRCh38 chr13: 19,527,899-24,671,591 , GRCh37.p13 chr13: 20,102,039-25,245,729 TPTE2-AS1, TNFRSF19, 112 more genes
    nsv7067798inversion1nstd229human GRCh38 chr13: 23,883,811-24,476,703 , GRCh37.p13 chr13: 24,457,950-25,050,841 CEND1P2, IPO7P2, 15 more genes
    nsv7063835inversion1nstd229human GRCh38 chr13: 22,751,036-26,757,157 , GRCh37.p13 chr13: 23,325,175-27,331,294 SPATA13, LOC105370122, 86 more genes
    nsv7062351inversion1nstd229human GRCh38 chr13: 22,876,629-24,898,116 , GRCh37.p13 chr13: 23,450,768-25,472,254 SGCG, SPATA13-AS1, 50 more genes
    nsv6932713copy number variation1nstd229human GRCh38 chr13: 19,442,684-24,587,300 , GRCh37.p13 chr13: 20,016,824-25,161,438 CEND1P2, MTCO3P2, 112 more genes
    nsv6927650copy number variation1nstd229human GRCh38 chr13: 24,324,801-24,329,700 , GRCh37.p13 chr13: 24,898,939-24,903,838 LINC00566, NUS1P3
    nsv6926544copy number variation1nstd229human GRCh38 chr13: 22,891,073-24,494,984 , GRCh37.p13 chr13: 23,465,212-25,069,122 LINC00621, LOC105370113, 35 more genes
    nsv6926248copy number variation1nstd229human GRCh38 chr13: 24,324,601-24,328,100 , GRCh37.p13 chr13: 24,898,739-24,902,238 NUS1P3
    nsv6924672copy number variation1nstd229human GRCh38 chr13: 22,843,141-24,510,019 , GRCh37.p13 chr13: 23,417,280-25,084,157 LOC107984585, LINC00566, 37 more genes
    nsv6637984copy number variation1nstd102humanUncertain significance GRCh37 chr13: 24,885,345-25,432,676 , GRCh38.p12 chr13: 24,311,207-24,858,538 LINC00566, CYCSP33, 20 more genes
    nsv6634440copy number variation1nstd102humanUncertain significance GRCh37 chr13: 23,981,973-24,963,501 , GRCh38.p12 chr13: 23,407,834-24,389,363 ANKRD20A19P, SPATA13, 19 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
    nsv6622129copy number variation1nstd224human GRCh37 chr13: 24,895,631-25,010,174 , GRCh38.p12 chr13: 24,321,493-24,436,036 PARP4, NUS1P3, 6 more genes
    nsv6622128copy number variation1nstd224human GRCh37 chr13: 24,771,519-25,020,887 , GRCh38.p12 chr13: 24,197,381-24,446,749 CEND1P2, PARP4, 8 more genes
    nsv6622126copy number variation1nstd224human GRCh37 chr13: 23,545,996-24,964,369 , GRCh38.p12 chr13: 22,971,857-24,390,231 TNFRSF19, C1QTNF9B, 29 more genes
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