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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971636insertion1nstd209human GRCh38 chr15: 74,639,701-74,639,701 , GRCh37.p13 chr15: 74,932,042-74,932,042 EDC3
    nsv5942982copy number variation1nstd209human GRCh38 chr15: 74,652,220-74,652,302 , GRCh37.p13 chr15: 74,944,561-74,944,643 EDC3
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5714675mobile element insertion1nstd211human GRCh38 chr15: 74,682,317-74,682,317 , GRCh37.p13 chr15: 74,974,658-74,974,658 EDC3
    nsv5708643mobile element insertion2nstd211human GRCh38 chr15: 74,658,654-74,658,654 , GRCh37.p13 chr15: 74,950,995-74,950,995 EDC3
    nsv5651838insertion1nstd207human GRCh38 chr15: 74,682,317-74,682,317 , GRCh37.p13 chr15: 74,974,658-74,974,658 EDC3
    nsv5558907sequence alteration1nstd206human GRCh38 chr15: 74,673,833-74,673,833 , GRCh37.p13 chr15: 74,966,174-74,966,174 EDC3
    nsv5552635insertion1nstd206human GRCh38 chr15: 74,661,873-74,661,923 , GRCh37.p13 chr15: 74,954,214-74,954,264 EDC3
    nsv5531549copy number variation1nstd206human GRCh38 chr15: 74,658,715-74,659,777 , GRCh37.p13 chr15: 74,951,056-74,952,118 EDC3
    nsv5525170copy number variation1nstd206human GRCh38 chr15: 74,675,348-74,678,523 , GRCh37.p13 chr15: 74,967,689-74,970,864 EDC3
    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
    nsv5365369translocation1nstd200human GRCh38 chr15: 74,696,082-74,696,082 , GRCh38 chr15: 74,699,655-74,699,655 , GRCh37.p13 chr15: 74,991,996-74,991,996 , GRCh37.p13 chr15: 74,988,423-74,988,423 EDC3
    nsv5365368translocation1nstd200human GRCh38 chr15: 74,696,066-74,696,066 , GRCh38 chr15: 74,700,035-74,700,035 , GRCh37.p13 chr15: 74,988,407-74,988,407 , GRCh37.p13 chr15: 74,992,376-74,992,376 EDC3
    nsv5159962mobile element insertion1nstd203human GRCh38 chr15: 74,679,882-74,679,904 , GRCh37.p13 chr15: 74,972,223-74,972,245 EDC3
    nsv5154457mobile element insertion1nstd203human GRCh38 chr15: 74,679,904-74,679,937 , GRCh37.p13 chr15: 74,972,245-74,972,278 EDC3
    nsv5009056copy number variation1nstd200human GRCh38 chr15: 74,653,014-74,654,315 , GRCh37.p13 chr15: 74,945,355-74,946,656 EDC3
    nsv4992343copy number variation1nstd200human GRCh38 chr15: 74,686,227-74,688,992 , GRCh37.p13 chr15: 74,978,568-74,981,333 EDC3
    nsv4992342copy number variation1nstd200human GRCh38 chr15: 74,658,652-74,659,806 , GRCh37.p13 chr15: 74,950,993-74,952,147 EDC3
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850093copy number variation1nstd200human GRCh37 chr15: 74,951,088-74,952,118 , GRCh38.p12 chr15: 74,658,747-74,659,777 EDC3
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