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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6974419copy number variation1nstd229human GRCh38 chr15: 43,243,257-43,255,473 , GRCh37.p13 chr15: 43,535,455-43,547,671 TGM5
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6966689copy number variation1nstd229human GRCh38 chr15: 43,124,367-43,284,900 , GRCh37.p13 chr15: 43,416,565-43,577,098 EPB42, TGM5, 6 more genes
    nsv6966482copy number variation1nstd229human GRCh38 chr15: 42,977,216-43,250,020 , GRCh37.p13 chr15: 43,269,414-43,542,218 SPCS2P1, TGM5, 6 more genes
    nsv6962222copy number variation1nstd229human GRCh38 chr15: 43,254,307-43,254,396 , GRCh37.p13 chr15: 43,546,505-43,546,594 TGM5
    nsv6962015copy number variation1nstd229human GRCh38 chr15: 43,246,196-43,272,233 , GRCh37.p13 chr15: 43,538,394-43,564,431 TGM5, ATP5PDP1
    nsv6496110copy number variation1nstd223human GRCh38 chr15: 43,175,921-43,650,339 , GRCh37.p13 chr15: 43,468,119-43,942,537 ADAL, EPB42, 19 more genes
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv5706417mobile element insertion1nstd211human GRCh38 chr15: 43,231,421-43,231,421 , GRCh37.p13 chr15: 43,523,619-43,523,619 TGM5
    nsv5503608copy number variation1nstd206human GRCh38 chr15: 43,231,421-43,231,607 , GRCh37.p13 chr15: 43,523,619-43,523,805 TGM5
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5314217copy number variation1nstd204human GRCh38.p13 chr15: 42,789,711-43,233,659 , GRCh37.p13 chr15: 43,081,909-43,525,857 FDPSP4, CCNDBP1, 9 more genes
    nsv5271224copy number variation1nstd204human GRCh38.p13 chr15: 42,789,601-43,233,700 , GRCh37.p13 chr15: 43,081,799-43,525,898 FDPSP10, RPS3AP47, 9 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4729554copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,135,272-43,744,542 , GRCh38.p12 chr15: 42,843,074-43,452,344 EPB42, FDPSP4, 16 more genes
    nsv4675221copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,420,601-44,198,616 , GRCh38.p12 chr15: 43,128,403-43,906,418 TGM5, CATSPER2P1, 38 more genes
    nsv4674906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,017,718-43,685,171 , GRCh38.p12 chr15: 42,725,520-43,392,973 UBR1, CDAN1, 17 more genes
    nsv4514949mobile element insertion1nstd166human GRCh37.p13 chr15: 43,530,890-43,530,890 , GRCh38.p12 chr15: 43,238,692-43,238,692 TGM5
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