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Items: 1 to 20 of 288

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097099copy number variation1nstd102humanUncertain significance GRCh37 chr7: 102,937,907-107,643,330 , GRCh38.p12 chr7: 103,297,460-108,002,885 SRPK2, SYPL1, 60 more genes
    nsv7052662inversion1nstd229human GRCh38 chr7: 102,309,147-103,483,817 , GRCh37.p13 chr7: 102,072,448-103,124,264 S100A11P1, RPL7AP39, 46 more genes
    nsv7040420inversion1nstd229human GRCh38 chr7: 101,445,712-104,173,878 , GRCh37.p13 chr7: 101,088,993-103,814,326 ALKBH4, RPS29P16, 54 more genes
    nsv6835123copy number variation1nstd229human GRCh38 chr7: 103,430,301-103,446,400 , GRCh37.p13 chr7: 103,070,748-103,086,847 SLC26A5, SLC26A5-AS1
    nsv6834025copy number variation1nstd229human GRCh38 chr7: 103,502,648-103,502,787 , GRCh37.p13 chr7: 103,143,095-103,143,234 SLC26A5-AS1, RELN
    nsv6833465copy number variation1nstd229human GRCh38 chr7: 103,459,101-103,465,500 , GRCh37.p13 chr7: 103,099,548-103,105,947 SLC26A5-AS1
    nsv6832799copy number variation1nstd229human GRCh38 chr7: 103,464,925-103,465,690 , GRCh37.p13 chr7: 103,105,372-103,106,137 SLC26A5-AS1
    nsv6831896copy number variation1nstd229human GRCh38 chr7: 103,501,967-103,511,505 , GRCh37.p13 chr7: 103,142,414-103,151,952 SLC26A5-AS1, RELN
    nsv6831681copy number variation1nstd229human GRCh38 chr7: 103,451,401-103,456,100 , GRCh37.p13 chr7: 103,091,848-103,096,547 SLC26A5-AS1
    nsv6831344copy number variation1nstd229human GRCh38 chr7: 103,452,495-103,456,083 , GRCh37.p13 chr7: 103,092,942-103,096,530 SLC26A5-AS1
    nsv6829369copy number variation1nstd229human GRCh38 chr7: 102,891,490-103,697,480 , GRCh37.p13 chr7: 102,531,937-103,337,927 RELN, DPY19L2P2, 18 more genes
    nsv6826148copy number variation1nstd229human GRCh38 chr7: 103,425,155-103,447,843 , GRCh37.p13 chr7: 103,065,602-103,088,290 SLC26A5, SLC26A5-AS1
    nsv6825872copy number variation1nstd229human GRCh38 chr7: 103,312,417-103,726,473 , GRCh37.p13 chr7: 102,952,864-103,366,920 SLC26A5, PMPCB, 7 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6617107copy number variation1nstd223human GRCh38 chr7: 103,452,501-103,456,100 , GRCh37.p13 chr7: 103,092,948-103,096,547 SLC26A5-AS1
    nsv6613781copy number variation1nstd223human GRCh38 chr7: 103,456,102-103,461,264 , GRCh37.p13 chr7: 103,096,549-103,101,711 SLC26A5-AS1
    nsv6613662copy number variation1nstd223human GRCh38 chr7: 103,464,925-103,465,690 , GRCh37.p13 chr7: 103,105,372-103,106,137 SLC26A5-AS1
    nsv6612322copy number variation1nstd223human GRCh38 chr7: 103,454,075-103,458,313 , GRCh37.p13 chr7: 103,094,522-103,098,760 SLC26A5-AS1
    nsv6611085copy number variation1nstd223human GRCh38 chr7: 103,459,146-103,465,521 , GRCh37.p13 chr7: 103,099,593-103,105,968 SLC26A5-AS1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
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