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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971169insertion1nstd209human GRCh38 chr12: 100,341,864-100,341,864 , GRCh37.p13 chr12: 100,735,642-100,735,642 SCYL2
    nsv5934275copy number variation1nstd209human GRCh38 chr12: 100,265,036-100,265,332 , GRCh37.p13 chr12: 100,658,814-100,659,110 SCYL2, DEPDC4
    nsv5929108copy number variation1nstd209human GRCh38 chr12: 100,282,181-100,282,481 , GRCh37.p13 chr12: 100,675,959-100,676,259 SCYL2
    nsv5714173mobile element insertion1nstd211human GRCh38 chr12: 100,341,879-100,341,879 , GRCh37.p13 chr12: 100,735,657-100,735,657 SCYL2
    nsv5695390mobile element insertion1nstd211human GRCh38 chr12: 100,341,864-100,341,864 , GRCh37.p13 chr12: 100,735,642-100,735,642 SCYL2
    nsv5659522insertion1nstd207human GRCh38 chr12: 100,294,521-100,294,521 , GRCh37.p13 chr12: 100,688,299-100,688,299 SCYL2
    nsv5645540insertion1nstd207human GRCh38 chr12: 100,294,428-100,294,428 , GRCh37.p13 chr12: 100,688,206-100,688,206 SCYL2
    nsv5644564insertion1nstd207human GRCh38 chr12: 100,294,713-100,294,713 , GRCh37.p13 chr12: 100,688,491-100,688,491 SCYL2
    nsv5586269copy number variation1nstd207human GRCh38 chr12: 100,282,181-100,282,481 , GRCh37.p13 chr12: 100,675,959-100,676,259 SCYL2
    nsv5534263insertion1nstd206human GRCh38 chr12: 100,295,794-100,295,827 , GRCh37.p13 chr12: 100,689,572-100,689,605 SCYL2
    nsv5510778copy number variation1nstd206human GRCh38 chr12: 100,268,324-100,268,378 , GRCh37.p13 chr12: 100,662,102-100,662,156 DEPDC4, SCYL2
    nsv5430286mobile element insertion1nstd206human GRCh38 chr12: 100,341,879-100,341,930 , GRCh37.p13 chr12: 100,735,657-100,735,708 SCYL2
    nsv5415015mobile element insertion1nstd206human GRCh38 chr12: 100,320,026-100,320,077 , GRCh37.p13 chr12: 100,713,804-100,713,855 SCYL2
    nsv5390945copy number variation1nstd186human GRCh37 chr12: 100,675,993-100,676,252 , GRCh38.p12 chr12: 100,282,215-100,282,474 SCYL2
    nsv5319904copy number variation1nstd204human GRCh38.p13 chr12: 100,282,045-100,282,638 , GRCh37.p13 chr12: 100,675,823-100,676,416 SCYL2
    nsv5265033copy number variation1nstd204human GRCh38.p13 chr12: 100,282,201-100,282,500 , GRCh37.p13 chr12: 100,675,979-100,676,278 SCYL2
    nsv5184551mobile element insertion1nstd203human GRCh38 chr12: 100,297,749-100,297,764 , GRCh37.p13 chr12: 100,691,527-100,691,542 SCYL2
    nsv5137463mobile element insertion1nstd203human GRCh38 chr12: 100,341,864-100,341,879 , GRCh37.p13 chr12: 100,735,642-100,735,657 SCYL2
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995272copy number variation1nstd200human GRCh38 chr12: 100,342,075-100,358,859 , GRCh37.p13 chr12: 100,735,853-100,752,637 SLC17A8, SCYL2
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