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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6834393copy number variation1nstd229human GRCh38 chr7: 38,944,248-39,960,814 , GRCh37.p13 chr7: 38,983,848-40,000,413 LOC100422519, LOC646999, 21 more genes
    nsv6830646copy number variation1nstd229human GRCh38 chr7: 39,656,501-41,139,000 , GRCh37.p13 chr7: 39,696,100-41,178,598 RALA, LOC105375242, 22 more genes
    nsv6828041copy number variation1nstd229human GRCh38 chr7: 39,718,782-39,751,749 , GRCh37.p13 chr7: 39,758,381-39,791,348 LINC00265
    nsv6827173copy number variation1nstd229human GRCh38 chr7: 39,751,073-39,751,621 , GRCh37.p13 chr7: 39,790,672-39,791,220 LINC00265
    nsv6826886copy number variation1nstd229human GRCh38 chr7: 39,753,001-39,757,900 , GRCh37.p13 chr7: 39,792,600-39,797,499 LINC00265
    nsv6825969copy number variation1nstd229human GRCh38 chr7: 39,780,497-39,785,602 , GRCh37.p13 chr7: 39,820,096-39,825,201 LINC00265
    nsv6824460copy number variation1nstd229human GRCh38 chr7: 39,755,957-39,770,264 , GRCh37.p13 chr7: 39,795,556-39,809,863 LINC00265, RNU6-719P
    nsv6824134copy number variation1nstd229human GRCh38 chr7: 39,764,940-39,765,231 , GRCh37.p13 chr7: 39,804,539-39,804,830 LINC00265
    nsv6823172copy number variation1nstd229human GRCh38 chr7: 39,756,607-39,988,428 , GRCh37.p13 chr7: 39,796,206-40,028,027 RN7SL496P, RWDD4P2, 8 more genes
    nsv6822535copy number variation1nstd229human GRCh38 chr7: 39,763,273-39,777,415 , GRCh37.p13 chr7: 39,802,872-39,817,014 RNU6-719P, LINC00265
    nsv6821745copy number variation1nstd229human GRCh38 chr7: 39,780,425-39,785,641 , GRCh37.p13 chr7: 39,820,024-39,825,240 LINC00265
    nsv6820233copy number variation1nstd229human GRCh38 chr7: 39,729,872-40,075,794 , GRCh37.p13 chr7: 39,769,471-40,115,393 RWDD4P2, CICP22, 8 more genes
    nsv6819127copy number variation1nstd229human GRCh38 chr7: 39,735,622-39,735,842 , GRCh37.p13 chr7: 39,775,221-39,775,441 LINC00265
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631947copy number variation1nstd224human GRCh37 chr7: 39,623,495-40,037,248 , GRCh38.p12 chr7: 39,583,896-39,997,649 YAE1, SSBP3P1, 12 more genes
    nsv6618944copy number variation1nstd223human GRCh38 chr7: 39,762,728-39,763,590 , GRCh37.p13 chr7: 39,802,327-39,803,189 LINC00265
    nsv6618453copy number variation1nstd223human GRCh38 chr7: 39,755,957-39,770,260 , GRCh37.p13 chr7: 39,795,556-39,809,859 LINC00265, RNU6-719P
    nsv6611127copy number variation1nstd223human GRCh38 chr7: 39,701,308-39,934,989 , GRCh37.p13 chr7: 39,740,907-39,974,588 CICP22, LOC100422519, 7 more genes
    nsv6610798copy number variation1nstd223human GRCh38 chr7: 39,763,661-39,764,814 , GRCh37.p13 chr7: 39,803,260-39,804,413 LINC00265
    nsv6610279copy number variation1nstd223human GRCh38 chr7: 39,718,782-39,751,749 , GRCh37.p13 chr7: 39,758,381-39,791,348 LINC00265
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