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Items: 1 to 20 of 311

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954079insertion1nstd209human GRCh38 chr7: 130,659,354-130,659,354 , GRCh37.p13 chr7: 130,344,194-130,344,194 , GRCh37.p13 chr7|NW_003871065.1: 338,585-338,585 COPG2
    nsv5920001copy number variation1nstd209human GRCh38 chr7: 130,576,876-130,577,936 , GRCh37.p13 chr7|NW_003871065.1: 256,107-257,167 , GRCh37.p13 chr7: 130,261,148-130,262,207 COPG2
    nsv5917089copy number variation1nstd209human GRCh38 chr7: 130,555,626-130,556,208 , GRCh37.p13 chr7|NW_003871065.1: 234,849-235,431 COPG2
    nsv5860257copy number variation1nstd209human GRCh38 chr7: 130,524,914-130,528,241 , GRCh37.p13 chr: NaN-NaN COPG2
    nsv5860041copy number variation1nstd209human GRCh38 chr7: 130,583,559-130,587,583 , GRCh37.p13 chr7: 130,267,830-130,271,852 , GRCh37.p13 chr7|NW_003871065.1: 262,790-266,814 COPG2
    nsv5850340copy number variation1nstd209human GRCh38 chr7: 130,537,761-130,542,081 , GRCh37.p13 chr: NaN-NaN COPG2IT1, COPG2
    nsv5711305mobile element insertion1nstd211human GRCh38 chr7: 130,521,045-130,521,045 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN COPG2
    nsv5641366insertion1nstd207human GRCh38 chr7: 130,591,123-130,591,123 , GRCh37.p13 chr7|NW_003871065.1: 270,354-270,354 COPG2
    nsv5641151insertion1nstd207human GRCh38 chr7: 130,591,453-130,591,453 , GRCh37.p13 chr7|NW_003871065.1: 270,684-270,684 , GRCh37.p13 chr7: 130,276,331-130,276,331 COPG2
    nsv5627458insertion1nstd207human GRCh38 chr7: 130,591,387-130,591,387 , GRCh37.p13 chr7|NW_003871065.1: 270,618-270,618 , GRCh37.p13 chr7: 130,276,262-130,276,262 COPG2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5492601copy number variation1nstd206human GRCh38 chr7: 130,530,828-130,535,406 , GRCh37.p13 chr: NaN-NaN COPG2
    nsv5492041copy number variation1nstd206human GRCh38 chr7: 130,582,215-130,587,544 , GRCh37.p13 chr7|NW_003871065.1: 261,446-266,775 , GRCh37.p13 chr7: 130,266,486-130,271,813 COPG2
    nsv5483524copy number variation1nstd206human GRCh38 chr7: 130,557,789-130,557,842 , GRCh37.p13 chr7|NW_003871065.1: 237,013-237,073 COPG2
    nsv5476027copy number variation1nstd206human GRCh38 chr7: 130,526,819-130,531,054 , GRCh37.p13 chr: NaN-NaN COPG2
    nsv5473968copy number variation1nstd206human GRCh38 chr7: 130,649,205-130,649,325 , GRCh37.p13 chr7|NW_003871065.1: 328,436-328,556 , GRCh37.p13 chr7: 130,334,047-130,334,167 COPG2
    nsv5394790mobile element insertion1nstd206human GRCh38 chr7: 130,521,045-130,521,096 , GRCh37.p13 chr: NaN-NaN COPG2
    nsv5371212translocation1nstd200human GRCh38 chr7: 130,642,247-130,642,247 , GRCh38 chr7: 130,642,385-130,642,385 , GRCh37.p13 chr7: 130,327,117-130,327,117 , GRCh37.p13 chr7|NW_003871065.1: 321,478-321,478 , GRCh37.p13 chr7|NW_003871065.1: 321,616-321,616 , GRCh37.p13 chr7: 130,327,255-130,327,255 COPG2
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5319308copy number variation1nstd204human GRCh38.p13 chr7: 130,582,146-130,587,559 , GRCh37.p13 chr7|NW_003871065.1: 261,377-266,790 , GRCh37.p13 chr7: 130,266,417-130,271,828 COPG2
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