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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7064943inversion1nstd229human GRCh38 chr15: 36,047,662-36,053,430 , GRCh37.p13 chr15: 36,339,863-36,345,631 LINC02853
    nsv7062966inversion1nstd229human GRCh38 chr15: 35,240,676-36,175,719 , GRCh37.p13 chr15: 35,532,877-36,467,920 LOC105370766, MIR4510, 8 more genes
    nsv6976467copy number variation1nstd229human GRCh38 chr15: 36,043,713-36,068,859 , GRCh37.p13 chr15: 36,335,914-36,361,060 LINC02853
    nsv6961323copy number variation1nstd229human GRCh38 chr15: 36,014,468-36,053,675 , GRCh37.p13 chr15: 36,306,669-36,345,876 LINC02853
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6132951copy number variation1nstd213human GRCh37 chr15: 36,330,000-36,450,001 , GRCh38.p12 chr15: 36,037,799-36,157,800 LINC02853, LOC102724214
    nsv6132950copy number variation1nstd213human GRCh37 chr15: 36,030,000-36,710,001 , GRCh38.p12 chr15: 35,737,799-36,417,800 DPH6-DT, LINC02853, 4 more genes
    nsv6132942copy number variation1nstd213human GRCh37 chr15: 36,334,101-36,676,516 , GRCh38.p12 chr15: 36,041,900-36,384,315 LINC02853, LOC102724214, 1 more genes
    nsv6027915copy number variation1nstd212human GRCh38 chr15: 36,044,421-36,044,474 , GRCh37.p13 chr15: 36,336,622-36,336,675 LINC02853
    nsv5976101insertion1nstd209human GRCh38 chr15: 36,044,437-36,044,437 , GRCh37.p13 chr15: 36,336,638-36,336,638 LINC02853
    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
    nsv5316435copy number variation1nstd204human GRCh38.p13 chr15: 36,046,096-36,046,224 , GRCh37.p13 chr15: 36,338,297-36,338,425 LINC02853
    nsv5001249copy number variation1nstd200human GRCh38 chr15: 36,046,100-36,046,221 , GRCh37.p13 chr15: 36,338,301-36,338,422 LINC02853
    nsv4855857copy number variation1nstd200human GRCh37 chr15: 36,338,301-36,338,422 , GRCh38.p12 chr15: 36,046,100-36,046,221 LINC02853
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 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
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4240085copy number variation1nstd166human GRCh37.p13 chr15: 36,306,669-36,345,871 , GRCh38.p12 chr15: 36,014,468-36,053,670 LINC02853
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