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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951924insertion1nstd209human GRCh38 chr10: 114,149,770-114,149,770 , GRCh37.p13 chr10: 115,909,529-115,909,529 CCDC186
    nsv5700191mobile element insertion1nstd211human GRCh38 chr10: 114,168,125-114,168,125 , GRCh37.p13 chr10: 115,927,884-115,927,884 CCDC186
    nsv5698232mobile element insertion1nstd211human GRCh38 chr10: 114,130,862-114,130,862 , GRCh37.p13 chr10: 115,890,621-115,890,621 CCDC186
    nsv5695619mobile element insertion1nstd211human GRCh38 chr10: 114,151,556-114,151,556 , GRCh37.p13 chr10: 115,911,315-115,911,315 CCDC186
    nsv5595454copy number variation1nstd207human GRCh38 chr10: 114,149,782-114,149,849 , GRCh37.p13 chr10: 115,909,541-115,909,608 CCDC186
    nsv5512013copy number variation1nstd206human GRCh38 chr10: 114,154,796-114,154,856 , GRCh37.p13 chr10: 115,914,555-115,914,615 CCDC186
    nsv5508242copy number variation1nstd206human GRCh38 chr10: 114,138,852-114,139,017 , GRCh37.p13 chr10: 115,898,611-115,898,776 CCDC186
    nsv5399195mobile element insertion1nstd206human GRCh38 chr10: 114,168,125-114,168,176 , GRCh37.p13 chr10: 115,927,884-115,927,935 CCDC186
    nsv5398821mobile element insertion1nstd206human GRCh38 chr10: 114,130,862-114,130,913 , GRCh37.p13 chr10: 115,890,621-115,890,672 CCDC186
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5125811mobile element insertion1nstd203human GRCh38 chr10: 114,151,547-114,151,556 , GRCh37.p13 chr10: 115,911,306-115,911,315 CCDC186
    nsv5121375mobile element insertion1nstd203human GRCh38 chr10: 114,151,548-114,151,556 , GRCh37.p13 chr10: 115,911,307-115,911,315 CCDC186
    nsv5120612mobile element insertion1nstd203human GRCh38 chr10: 114,151,552-114,151,556 , GRCh37.p13 chr10: 115,911,311-115,911,315 CCDC186
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4977040copy number variation1nstd200human GRCh38 chr10: 114,131,395-114,131,463 , GRCh37.p13 chr10: 115,891,154-115,891,222 CCDC186
    nsv4880587inversion1nstd200human GRCh37 chr10: 115,288,028-117,482,906 , GRCh38.p12 chr10: 113,528,269-115,723,396 , NHLRC2, 31 more genes
    nsv4613840copy number variation1nstd183human GRCh37 chr10: 115,870,936-115,882,676 , GRCh38.p12 chr10: 114,111,177-114,122,917 CCDC186, UBE2V1P5, 1 more genes
    nsv4611485copy number variation2nstd183human GRCh37 chr10: 115,881,078-115,885,723 , GRCh38.p12 chr10: 114,121,319-114,125,964 CCDC186
    nsv4492605mobile element insertion1nstd166human GRCh37.p13 chr10: 115,911,306-115,911,306 , GRCh38.p12 chr10: 114,151,547-114,151,547 CCDC186
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
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