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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5725371mobile element insertion1nstd211human GRCh38 chr10: 101,795,939-101,795,939 , GRCh37.p13 chr10: 103,555,696-103,555,696 OGA
    nsv5713628mobile element insertion1nstd211human GRCh38 chr10: 101,808,644-101,808,644 , GRCh37.p13 chr10: 103,568,401-103,568,401 OGA
    nsv5410650mobile element insertion1nstd206human GRCh38 chr10: 101,804,220-101,804,248 , GRCh37.p13 chr10: 103,563,977-103,564,005 OGA
    nsv5406987mobile element insertion1nstd206human GRCh38 chr10: 101,808,644-101,808,695 , GRCh37.p13 chr10: 103,568,401-103,568,452 OGA
    nsv5206804mobile element deletion1nstd204human GRCh38.p13 chr10: 101,814,037-101,814,349 , GRCh37.p13 chr10: 103,573,794-103,574,106 OGA
    nsv5136501mobile element insertion1nstd203human GRCh38 chr10: 101,808,631-101,808,644 , GRCh37.p13 chr10: 103,568,388-103,568,401 OGA
    nsv5127786mobile element insertion1nstd203human GRCh38 chr10: 101,815,963-101,816,001 , GRCh37.p13 chr10: 103,575,720-103,575,758 OGA
    nsv5127548mobile element insertion1nstd203human GRCh38 chr10: 101,798,325-101,798,336 , GRCh37.p13 chr10: 103,558,082-103,558,093 OGA
    nsv4973985copy number variation1nstd200human GRCh38 chr10: 101,791,930-101,838,328 , GRCh37.p13 chr10: 103,551,687-103,598,085 OGA, KCNIP2-AS1, 1 more genes
    nsv4837880copy number variation1nstd200human GRCh37 chr10: 103,551,687-103,598,085 , GRCh38.p12 chr10: 101,791,930-101,838,328 OGA, KCNIP2-AS1, 1 more genes
    nsv4774818mobile element deletion1nstd200human GRCh37 chr10: 103,573,803-103,574,098 , GRCh38.p12 chr10: 101,814,046-101,814,341 OGA
    nsv4680797copy number variation1nstd189human GRCh37.p13 chr10: 102,835,750-103,653,301 , GRCh38.p12 chr10: 101,075,993-101,893,544 , FGF8, 28 more genes
    nsv4485491mobile element insertion1nstd166human GRCh37.p13 chr10: 103,558,082-103,558,082 , GRCh38.p12 chr10: 101,798,325-101,798,325 OGA
    nsv4482620mobile element insertion1nstd166human GRCh37.p13 chr10: 103,568,388-103,568,388 , GRCh38.p12 chr10: 101,808,631-101,808,631 OGA
    nsv4349819copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,822,575-103,558,868 , GRCh38.p12 chr10: 101,062,818-101,799,111 LBX1, TLX1, 22 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4191783copy number variation1nstd166human GRCh37.p13 chr10: 103,543,000-103,553,000 , GRCh38.p12 chr10: 101,783,243-101,793,243 OGA, NPM3
    nsv4185203copy number variation1nstd166human GRCh37.p13 chr10: 103,392,389-103,550,550 , GRCh38.p12 chr10: 101,632,632-101,790,793 , FGF8, 6 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
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