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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947330copy number variation1nstd209human GRCh38 chr13: 63,685,279-63,801,129 , GRCh37.p13 chr13: 64,259,412-64,375,262 OR7E156P, RNU6-81P, 3 more genes
    nsv5859710copy number variation2nstd209human GRCh38 chr13: 63,775,984-63,791,827 , GRCh37.p13 chr13: 64,350,117-64,365,960 RNU6-81P
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5564035sequence alteration1nstd206human GRCh38 chr13: 63,739,541-63,842,183 , GRCh37.p13 chr13: 64,313,674-64,416,316 OR7E104P, OR7E156P, 5 more genes
    nsv5508335copy number variation1nstd206human GRCh38 chr13: 63,685,279-63,801,130 , GRCh37.p13 chr13: 64,259,412-64,375,263 LINC00395, OR7E156P, 3 more genes
    nsv5503228copy number variation1nstd206human GRCh38 chr13: 63,764,053-63,833,106 , GRCh37.p13 chr13: 64,338,186-64,407,239 PPP1R2P10, RNU6-81P, 2 more genes
    nsv5502458copy number variation1nstd206human GRCh38 chr13: 63,518,387-63,954,542 , GRCh37.p13 chr13: 64,092,520-64,528,675 LOC105377815, LOC105370236, 10 more genes
    nsv5502222copy number variation1nstd206human GRCh38 chr13: 63,726,106-63,827,106 , GRCh37.p13 chr13: 64,300,239-64,401,239 OR7E156P, PPP1R2P10, 5 more genes
    nsv5497177copy number variation1nstd206human GRCh38 chr13: 63,756,106-63,824,176 , GRCh37.p13 chr13: 64,330,239-64,398,309 RNU6-81P, PPP1R2P10
    nsv5494309copy number variation1nstd206human GRCh38 chr13: 63,662,643-63,935,349 , GRCh37.p13 chr13: 64,236,776-64,509,482 LOC105370235, OR7E104P, 9 more genes
    nsv5305621copy number variation1nstd204human GRCh37.p13 chr13: 64,259,408-64,375,272 , GRCh38.p13 chr13: 63,685,275-63,801,139 OR7E156P, RNU6-81P, 3 more genes
    nsv5275531copy number variation1nstd204human GRCh38.p13 chr13: 63,784,199-63,785,674 , GRCh37.p13 chr13: 64,358,332-64,359,807 RNU6-81P
    nsv5269186copy number variation1nstd204human GRCh38.p13 chr13: 63,749,214-63,814,230 , GRCh37.p13 chr13: 64,323,347-64,388,363 RNU6-81P, PPP1R2P10
    nsv5268738copy number variation1nstd204human GRCh38.p13 chr13: 63,760,671-63,821,162 , GRCh37.p13 chr13: 64,334,804-64,395,295 PPP1R2P10, RNU6-81P
    nsv5039398inversion1nstd200human GRCh38 chr13: 63,499,867-68,921,282 , GRCh37.p13 chr13: 64,074,000-69,495,414 RN7SL761P, STARP1, 55 more genes
    nsv5034873inversion1nstd200human GRCh38 chr13: 55,150,893-76,780,363 , GRCh37.p13 chr13: 55,725,028-77,354,498 , PRR20C, 199 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4872325inversion1nstd200human GRCh37 chr13: 55,725,028-77,354,498 , GRCh38.p12 chr13: 55,150,893-76,780,363 , OR7E111P, 199 more genes
    nsv4871291inversion1nstd200human GRCh37 chr13: 64,074,000-69,495,413 , GRCh38.p12 chr13: 63,499,867-68,921,281 NFYAP1, RN7SL761P, 55 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
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