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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5005262copy number variation1nstd200human GRCh38 chr15: 34,746,264-34,886,834 , GRCh37.p13 chr15: 35,038,465-35,179,035 ACTC1, AQR, 4 more genes
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4682802copy number variation2nstd102humanUncertain significance GRCh37 chr15: 35,080,829-35,087,019 , GRCh38.p12 chr15: 34,788,628-34,794,818 GJD2-DT, ACTC1
    nsv4680465copy number variation1nstd189human GRCh37.p13 chr15: 34,771,762-35,203,705 , GRCh38.p12 chr15: 34,479,561-34,911,504 ACTC1, AQR, 11 more genes
    nsv4679586copy number variation1nstd189human GRCh37.p13 chr15: 35,059,342-35,171,068 , GRCh38.p12 chr15: 34,767,141-34,878,867 ACTC1, AQR, 3 more genes
    nsv4675702copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,675,452-35,689,958 , GRCh38.p12 chr15: 31,383,249-35,397,757 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 AVEN, PRELID1P4, 113 more genes
    nsv4675391copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053 TPST2P1, AVEN, 65 more genes
    nsv4674936copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278 SNORD115-48, MIR4509-2, 330 more genes
    nsv4625075copy number variation1nstd183human GRCh37 chr15: 34,855,818-35,147,345 , GRCh38.p12 chr15: 34,563,617-34,855,144 ACTC1, AQR, 6 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4429259copy number variation1nstd174human GRCh37 chr15: 34,862,247-35,142,566 , GRCh38.p12 chr15: 34,570,046-34,850,365 ACTC1, AQR, 6 more genes
    nsv4425673copy number variation1nstd174human GRCh37 chr15: 32,896,350-35,372,508 , GRCh38.p12 chr15: 32,604,149-35,080,307 , ACTC1, 50 more genes
    nsv4240076copy number variation1nstd166human GRCh37.p13 chr15: 34,802,630-35,336,031 , GRCh38.p12 chr15: 34,510,429-35,043,830 LOC105370764, GJD2, 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
    nsv3921227copy number variation1nstd102humanPathogenic NCBI36 chr15: 30,686,791-33,279,922 , GRCh37 chr15: 32,899,499-35,492,630 , GRCh38 chr15: 32,607,298-35,200,429 TMCO5B, PRELID1P4, 52 more genes
    nsv3921026copy number variation1nstd102humanPathogenic NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505 SNORD116-17, LOC100996670, 303 more genes
    nsv3920384copy number variation1nstd102humanPathogenic NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269 PGBD4, LOC105370763, 113 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919055copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,880,216-39,572,605 , NCBI36 chr15: 32,667,508-37,359,897 , GRCh38 chr15: 34,588,015-39,280,404 DPH6, NUTF2P6, 56 more genes
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