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Items: 1 to 20 of 937

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141165insertion1nstd232human GRCh37.p13 chr13: 24,764,327-24,764,327 , GRCh38.p12 chr13: 24,190,188-24,190,188 SPATA13
    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
    nsv7077160inversion1nstd229human GRCh38 chr13: 24,006,946-24,039,849 , GRCh37.p13 chr13: 24,581,085-24,613,988 SPATA13
    nsv7073256inversion1nstd229human GRCh38 chr13: 19,714,497-24,851,015 , GRCh37.p13 chr13: 20,288,637-25,425,153 SPATA13, IFT88, 114 more genes
    nsv7072061inversion1nstd229human GRCh38 chr13: 23,905,845-24,264,432 , GRCh37.p13 chr13: 24,479,984-24,838,570 MIR2276, LOC105370115, 4 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
    nsv7070217inversion1nstd229human GRCh38 chr13: 23,906,820-24,032,027 , GRCh37.p13 chr13: 24,480,959-24,606,166 ANKRD20A19P, SPATA13, 1 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
    nsv7066817inversion1nstd229human GRCh38 chr13: 24,083,043-24,093,430 , GRCh37.p13 chr13: 24,657,182-24,667,569 SPATA13
    nsv7064659inversion1nstd229human GRCh38 chr13: 21,701,072-24,290,855 , GRCh37.p13 chr13: 22,275,211-24,864,993 ANKRD20A19P, SPATA13, 40 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
    nsv7063622inversion1nstd229human GRCh38 chr13: 24,028,457-24,028,575 , GRCh37.p13 chr13: 24,602,596-24,602,714 SPATA13
    nsv7062852inversion1nstd229human GRCh38 chr13: 24,082,264-24,090,657 , GRCh37.p13 chr13: 24,656,403-24,664,796 SPATA13
    nsv7062351inversion1nstd229human GRCh38 chr13: 22,876,629-24,898,116 , GRCh37.p13 chr13: 23,450,768-25,472,254 SGCG, SPATA13-AS1, 50 more genes
    nsv7062192inversion1nstd229human GRCh38 chr13: 23,996,080-24,023,823 , GRCh37.p13 chr13: 24,570,219-24,597,962 SPATA13
    nsv7058998inversion1nstd229human GRCh38 chr13: 24,080,726-24,306,810 , GRCh37.p13 chr13: 24,654,865-24,880,948 SPATA13-AS1, SPATA13, 3 more genes
    nsv6937762copy number variation1nstd229human GRCh38 chr13: 24,133,601-24,166,500 , GRCh37.p13 chr13: 24,707,740-24,740,639 SPATA13, MIR2276
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