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Items: 1 to 20 of 689

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139048copy number variation1nstd232human GRCh37.p13 chr8: 144,422,388-144,422,450 , GRCh38.p12 chr8: 143,340,218-143,340,280 TOP1MT
    nsv7098166copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,391,611-144,417,031 , GRCh38.p12 chr8: 143,309,441-143,334,861 TOP1MT
    nsv7076667inversion1nstd229human GRCh38 chr8: 143,290,829-143,355,763 , GRCh37.p13 chr8: 144,372,999-144,437,933 RNU6-220P, ZNF696, 1 more genes
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7060207inversion1nstd229human GRCh38 chr8: 143,324,640-143,375,537 , GRCh37.p13 chr8: 144,406,810-144,457,707 RNU6-220P, RHPN1, 2 more genes
    nsv6873592copy number variation1nstd229human GRCh38 chr8: 143,297,334-143,319,447 , GRCh37.p13 chr8: 144,379,504-144,401,617 TOP1MT, ZNF696
    nsv6871840copy number variation1nstd229human GRCh38 chr8: 143,273,127-143,593,659 , GRCh37.p13 chr8: 144,355,297-144,675,829 MAFA-AS1, SNORD149, 16 more genes
    nsv6871698copy number variation1nstd229human GRCh38 chr8: 143,329,625-143,329,715 , GRCh37.p13 chr8: 144,411,795-144,411,885 TOP1MT
    nsv6870026copy number variation1nstd229human GRCh38 chr8: 143,358,701-143,389,700 , GRCh37.p13 chr8: 144,440,871-144,471,870 TOP1MT, RHPN1-AS1, 1 more genes
    nsv6869585copy number variation1nstd229human GRCh38 chr8: 143,348,922-143,348,952 , GRCh37.p13 chr8: 144,431,092-144,431,122 TOP1MT, RNU6-220P
    nsv6867072copy number variation1nstd229human GRCh38 chr8: 143,242,548-143,329,567 , GRCh37.p13 chr8: 144,324,718-144,411,737 GLI4, MINCR, 3 more genes
    nsv6863714copy number variation1nstd229human GRCh38 chr8: 143,343,017-143,361,218 , GRCh37.p13 chr8: 144,425,187-144,443,388 RNU6-220P, TOP1MT
    nsv6862776copy number variation1nstd229human GRCh38 chr8: 143,312,519-143,316,970 , GRCh37.p13 chr8: 144,394,689-144,399,140 TOP1MT
    nsv6862669copy number variation1nstd229human GRCh38 chr8: 143,360,283-143,360,330 , GRCh37.p13 chr8: 144,442,453-144,442,500 TOP1MT
    nsv6862032copy number variation1nstd229human GRCh38 chr8: 143,347,240-143,353,640 , GRCh37.p13 chr8: 144,429,410-144,435,810 TOP1MT, RNU6-220P
    nsv6861848copy number variation1nstd229human GRCh38 chr8: 143,316,051-143,357,839 , GRCh37.p13 chr8: 144,398,221-144,440,009 RNU6-220P, TOP1MT
    nsv6860477copy number variation1nstd229human GRCh38 chr8: 143,358,718-143,389,695 , GRCh37.p13 chr8: 144,440,888-144,471,865 TOP1MT, RHPN1-AS1, 1 more genes
    nsv6860178copy number variation1nstd229human GRCh38 chr8: 143,332,697-143,396,956 , GRCh37.p13 chr8: 144,414,867-144,479,126 RHPN1-AS1, RNU6-220P, 2 more genes
    nsv6637661copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,895,666-144,568,446 , GRCh38.p12 chr8: 142,814,250-143,486,276 LY6L, ZC3H3, 26 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
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