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Items: 1 to 20 of 122

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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
    nsv6975585copy number variation1nstd229human GRCh38 chr15: 43,624,353-43,787,662 , GRCh37.p13 chr15: 43,916,551-44,079,860 RNU6-610P, ELL3, 11 more genes
    nsv6971514copy number variation1nstd229human GRCh38 chr15: 43,760,926-43,883,619 , GRCh37.p13 chr15: 44,053,124-44,175,817 PDIA3, SERF2-C15ORF63, 9 more genes
    nsv6966735copy number variation1nstd229human GRCh38 chr15: 43,770,070-43,771,124 , GRCh37.p13 chr15: 44,062,268-44,063,322 PDIA3, ELL3
    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
    nsv6025962copy number variation1nstd212human GRCh38 chr15: 43,776,358-43,776,417 , GRCh37.p13 chr15: 44,068,556-44,068,615 SERF2, ELL3
    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
    nsv5355912translocation1nstd200human GRCh38 chr15: 43,774,179-43,774,179 , GRCh38 chr12: 50,314,602-50,314,602 , GRCh37.p13 chr12: 50,708,385-50,708,385 , GRCh37.p13 chr15: 44,066,377-44,066,377 ELL3
    nsv5339512translocation1nstd200human GRCh37 chr15: 44,066,191-44,066,191 , GRCh37 chr12: 50,708,371-50,708,371 , GRCh38.p12 chr12: 50,314,588-50,314,588 , GRCh38.p12 chr15: 43,773,993-43,773,993 ELL3
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001514copy number variation1nstd200human GRCh38 chr15: 43,772,321-43,772,511 , GRCh37.p13 chr15: 44,064,519-44,064,709 ELL3, PDIA3
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 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
    nsv4626241copy number variation2nstd183human GRCh37 chr15: 44,067,764-44,067,808 , GRCh38.p12 chr15: 43,775,566-43,775,610 ELL3, SERF2
    nsv4624606copy number variation1nstd183human GRCh37 chr15: 44,067,563-44,067,808 , GRCh38.p12 chr15: 43,775,365-43,775,610 ELL3, SERF2
    nsv4618727copy number variation1nstd183human GRCh37 chr15: 44,067,764-44,067,980 , GRCh38.p12 chr15: 43,775,566-43,775,782 SERF2, ELL3
    nsv4383436copy number variation1nstd173human GRCh37 chr15: 43,851,399-44,325,282 , GRCh38.p12 chr15: 43,559,201-44,033,084 PPIP5K1P1-CATSPER2, RNU6-554P, 24 more genes
    nsv4381260copy number variation1nstd173human GRCh37 chr15: 44,054,738-44,191,082 , GRCh38.p12 chr15: 43,762,540-43,898,884 SERF2-C15ORF63, SERINC4, 9 more genes
    nsv4372500copy number variation1nstd173human GRCh37 chr15: 43,992,627-44,198,616 , GRCh38.p12 chr15: 43,700,429-43,906,418 WDR76, ELL3, 13 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
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