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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139952copy number variation1nstd232human GRCh37.p13 chr13: 25,456,271-25,456,394 , GRCh38.p12 chr13: 24,882,133-24,882,256 CENPJ, RNF17
    nsv7139456copy number variation1nstd232human GRCh37.p13 chr13: 25,458,221-25,458,297 , GRCh38.p12 chr13: 24,884,083-24,884,159 CENPJ, RNF17
    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
    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
    nsv7069640inversion1nstd229human GRCh38 chr13: 24,885,385-24,899,585 , GRCh37.p13 chr13: 25,459,523-25,473,723 RNF17, CENPJ
    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
    nsv6928436copy number variation1nstd229human GRCh38 chr13: 24,885,820-24,890,262 , GRCh37.p13 chr13: 25,459,958-25,464,400 RNF17, CENPJ
    nsv6924720copy number variation1nstd229human GRCh38 chr13: 24,899,981-24,900,169 , GRCh37.p13 chr13: 25,474,119-25,474,307 CENPJ
    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
    nsv6595379inversion1nstd223human GRCh38 chr13: 24,580,561-24,968,592 , GRCh37.p13 chr13: 25,154,699-25,542,730 CENPJ, RNY1P7, 12 more genes
    nsv6594018inversion1nstd223human GRCh38 chr13: 24,595,891-24,953,310 , GRCh37.p13 chr13: 25,170,029-25,527,448 TPTE2P6, IRX1P1, 12 more genes
    nsv6593859inversion1nstd223human GRCh38 chr13: 22,904,574-24,978,653 , GRCh37.p13 chr13: 23,478,713-25,552,791 TPTE2P6, ANKRD20A19P, 52 more genes
    nsv6591359inversion1nstd223human GRCh38 chr13: 24,595,318-24,953,345 , GRCh37.p13 chr13: 25,169,456-25,527,483 TPTE2P6, IRX1P1, 12 more genes
    nsv6589951inversion1nstd223human GRCh38 chr13: 24,612,703-25,013,183 , GRCh37.p13 chr13: 25,186,841-25,587,321 RNF17, RPL26P34, 12 more genes
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