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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
    nsv5893615copy number variation1nstd209human GRCh38 chr6: 33,281,307-33,284,872 , GRCh37.p13 chr6: 33,249,084-33,252,649 WDR46
    nsv5844939copy number variation1nstd209human GRCh38 chr6: 33,281,487-33,282,836 , GRCh37.p13 chr6: 33,249,264-33,250,613 WDR46
    nsv5462262copy number variation1nstd206human GRCh38 chr6: 33,281,310-33,284,873 , GRCh37.p13 chr6: 33,249,087-33,252,650 WDR46
    nsv5455396copy number variation1nstd206human GRCh38 chr6: 33,281,254-33,282,865 , GRCh37.p13 chr6: 33,249,031-33,250,642 WDR46
    nsv5378374translocation1nstd200human GRCh38 chr6: 33,284,954-33,284,954 , GRCh38 chr6: 33,282,808-33,282,808 , GRCh37.p13 chr6: 33,250,585-33,250,585 , GRCh37.p13 chr6: 33,252,731-33,252,731 WDR46
    nsv5231786copy number variation1nstd204human GRCh38.p13 chr6: 33,016,601-33,499,100 , GRCh37.p13 chr6: 32,984,378-33,466,877 COL11A2, RXRB, 39 more genes
    nsv4940761copy number variation1nstd200human GRCh38 chr6: 33,283,432-33,284,066 , GRCh37.p13 chr6: 33,251,209-33,251,843 WDR46
    nsv4940760copy number variation1nstd200human GRCh38 chr6: 33,280,893-33,282,277 , GRCh37.p13 chr6: 33,248,670-33,250,054 WDR46
    nsv4934592copy number variation1nstd200human GRCh38 chr6: 33,252,284-33,301,488 , GRCh37.p13 chr6: 33,220,061-33,269,265 RPS18, RGL2, 8 more genes
    nsv4815917copy number variation1nstd200human GRCh37 chr6: 33,249,056-33,250,609 , GRCh38.p12 chr6: 33,281,279-33,282,832 WDR46
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4682849copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926 RPL35AP4, RGL2, 29 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4593570copy number variation2nstd183human GRCh37 chr6: 33,249,085-33,250,420 , GRCh38.p12 chr6: 33,281,308-33,282,643 WDR46
    nsv4593569copy number variation1nstd183human GRCh37 chr6: 33,222,163-33,256,397 , GRCh38.p12 chr6: 33,254,386-33,288,620 RPS18, VPS52, 6 more genes
    nsv4451881copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926 COL11A2, HSD17B8, 29 more genes
    nsv4409836copy number variation1nstd174human GRCh37 chr6: 33,248,658-33,250,582 , GRCh38.p12 chr6: 33,280,881-33,282,805 WDR46
    nsv4381952copy number variation1nstd173human GRCh37 chr6: 33,222,841-33,259,562 , GRCh38.p12 chr6: 33,255,064-33,291,785 RGL2, VPS52, 7 more genes
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