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Items: 1 to 20 of 514

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094399copy number variation1nstd102humanPathogenic GRCh37 chr13: 23,898,487-24,463,459 , GRCh38.p12 chr13: 23,324,348-23,889,320 LOC105370113, TNFRSF19, 9 more genes
    nsv7094398copy number variation1nstd102humanUncertain significance GRCh37 chr13: 23,777,834-23,985,378 , GRCh38.p12 chr13: 23,203,695-23,411,239 RNU6-58P, RPLP1P13, 5 more genes
    nsv7094239copy number variation1nstd102humanPathogenic GRCh37 chr13: 23,927,914-23,985,388 , GRCh38.p12 chr13: 23,353,775-23,411,249 RPLP1P13, SACS
    nsv7094238copy number variation2nstd102humanUncertain significance GRCh37 chr13: 23,667,335-24,463,459 , GRCh38.p12 chr13: 23,093,196-23,889,320 LINC00327, SACS, 16 more genes
    nsv7094070copy number variation1nstd102humanPathogenic GRCh37 chr13: 23,903,991-23,905,304 , GRCh38.p12 chr13: 23,329,852-23,331,165 SACS
    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
    nsv7064659inversion1nstd229human GRCh38 chr13: 21,701,072-24,290,855 , GRCh37.p13 chr13: 22,275,211-24,864,993 ANKRD20A19P, SPATA13, 40 more genes
    nsv7064429inversion1nstd229human GRCh38 chr13: 23,368,907-23,854,179 , GRCh37.p13 chr13: 23,943,046-24,428,318 MTCO3P2, LOC105370113, 6 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
    nsv7060653inversion1nstd229human GRCh38 chr13: 23,015,813-23,618,700 , GRCh37.p13 chr13: 23,589,952-24,192,839 SACS-AS1, TNFRSF19, 11 more genes
    nsv6936697copy number variation1nstd229human GRCh38 chr13: 23,356,708-23,357,091 , GRCh37.p13 chr13: 23,930,847-23,931,230 SACS
    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
    nsv6927031copy number variation1nstd229human GRCh38 chr13: 23,354,319-23,354,487 , GRCh37.p13 chr13: 23,928,458-23,928,626 SACS
    nsv6926880copy number variation1nstd229human GRCh38 chr13: 22,387,384-23,519,592 , GRCh37.p13 chr13: 22,961,523-24,093,731 RNU6-58P, LOC105370112, 21 more genes
    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
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