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Items: 1 to 20 of 145

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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
    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
    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
    nsv6035575copy number variation1nstd212human GRCh38 chr15: 43,191,201-43,191,346 , GRCh37.p13 chr15: 43,483,399-43,483,544 CCNDBP1
    nsv6030039copy number variation1nstd212human GRCh38 chr15: 43,193,341-43,193,397 , GRCh37.p13 chr15: 43,485,539-43,485,595 CCNDBP1
    nsv6020473copy number variation1nstd212human GRCh38 chr15: 43,185,573-43,186,200 , GRCh37.p13 chr15: 43,477,771-43,478,398 TMEM62, CCNDBP1
    nsv5508215copy number variation1nstd206human GRCh38 chr15: 43,191,181-43,191,365 , GRCh37.p13 chr15: 43,483,379-43,483,563 CCNDBP1
    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
    nsv5264271copy number variation1nstd204human GRCh38.p13 chr15: 43,181,380-43,187,370 , GRCh37.p13 chr15: 43,473,578-43,479,568 CCNDBP1, TMEM62
    nsv5153130mobile element insertion1nstd203human GRCh38 chr15: 43,187,067-43,187,084 , GRCh37.p13 chr15: 43,479,265-43,479,282 CCNDBP1
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005323copy number variation1nstd200human GRCh38 chr15: 43,190,556-43,191,160 , GRCh37.p13 chr15: 43,482,754-43,483,358 CCNDBP1
    nsv5001502copy number variation1nstd200human GRCh38 chr15: 43,192,081-43,192,166 , GRCh37.p13 chr15: 43,484,279-43,484,364 CCNDBP1
    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
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