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Items: 1 to 20 of 344

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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
    nsv7071840inversion1nstd229human GRCh38 chr13: 24,420,212-24,937,611 , GRCh37.p13 chr13: 24,994,350-25,511,749 ATP12A, LOC101927375, 16 more genes
    nsv7071412inversion1nstd229human GRCh38 chr13: 24,410,246-24,981,742 , GRCh37.p13 chr13: 24,984,384-25,555,880 CLUHP9, RNY1P7, 17 more genes
    nsv7070728inversion1nstd229human GRCh38 chr13: 24,413,769-24,978,194 , GRCh37.p13 chr13: 24,987,907-25,552,332 PARP4, LOC105370117, 17 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
    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
    nsv7061008inversion1nstd229human GRCh38 chr13: 24,612,704-25,013,150 , GRCh37.p13 chr13: 25,186,842-25,587,288 IRX1P1, CENPJ, 12 more genes
    nsv6936218copy number variation1nstd229human GRCh38 chr13: 24,695,492-24,760,603 , GRCh37.p13 chr13: 25,269,630-25,334,741 LOC105370118, RNY1P7, 6 more genes
    nsv6934189copy number variation1nstd229human GRCh38 chr13: 24,696,424-24,696,745 , GRCh37.p13 chr13: 25,270,562-25,270,883 ATP12A
    nsv6933642copy number variation1nstd229human GRCh38 chr13: 24,693,981-24,694,027 , GRCh37.p13 chr13: 25,268,119-25,268,165 ATP12A
    nsv6932375copy number variation1nstd229human GRCh38 chr13: 24,558,443-24,762,902 , GRCh37.p13 chr13: 25,132,581-25,337,040 RPL26P34, RNF17, 10 more genes
    nsv6926320copy number variation1nstd229human GRCh38 chr13: 24,692,842-24,693,038 , GRCh37.p13 chr13: 25,266,980-25,267,176 ATP12A
    nsv6924299copy number variation1nstd229human GRCh38 chr13: 24,677,801-24,772,900 , GRCh37.p13 chr13: 25,251,939-25,347,038 LOC105370118, ATP12A, 6 more genes
    nsv6919314copy number variation1nstd229human GRCh38 chr13: 24,710,140-24,722,227 , GRCh37.p13 chr13: 25,284,278-25,296,365 ATP12A, LOC105370118
    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
    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
    nsv6622135copy number variation2nstd224human GRCh37 chr13: 25,272,795-25,327,320 , GRCh38.p12 chr13: 24,698,657-24,753,182 ATP12A, RNF17, 6 more genes
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