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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7074163inversion1nstd229human GRCh38 chr20: 5,833,272-5,855,274 , GRCh37.p13 chr20: 5,813,918-5,835,920 SHLD1
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7063264inversion1nstd229human GRCh38 chr20: 5,408,131-5,833,273 , GRCh37.p13 chr20: 5,388,777-5,813,919 RPS18P1, LOC643406, 8 more genes
    nsv7063012inversion1nstd229human GRCh38 chr20: 5,360,837-5,792,198 , GRCh37.p13 chr20: 5,341,483-5,772,844 RPS18P1, LOC107985411, 8 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7060087inversion1nstd229human GRCh38 chr20: 5,513,910-5,805,219 , GRCh37.p13 chr20: 5,494,556-5,785,865 SHLD1, LOC105372514, 3 more genes
    nsv7017567copy number variation1nstd229human GRCh38 chr20: 5,755,137-5,796,786 , GRCh37.p13 chr20: 5,735,783-5,777,432 SHLD1
    nsv7016503copy number variation1nstd229human GRCh38 chr20: 5,777,001-5,783,900 , GRCh37.p13 chr20: 5,757,647-5,764,546 SHLD1
    nsv7015076copy number variation1nstd229human GRCh38 chr20: 5,542,196-5,804,666 , GRCh37.p13 chr20: 5,522,842-5,785,312 EIF4EP1, SHLD1, 2 more genes
    nsv7014379copy number variation1nstd229human GRCh38 chr20: 5,809,305-5,810,070 , GRCh37.p13 chr20: 5,789,951-5,790,716 SHLD1
    nsv7014087copy number variation1nstd229human GRCh38 chr20: 5,759,241-5,761,855 , GRCh37.p13 chr20: 5,739,887-5,742,501 SHLD1
    nsv7012376copy number variation1nstd229human GRCh38 chr20: 5,841,278-5,841,619 , GRCh37.p13 chr20: 5,821,924-5,822,265 SHLD1
    nsv7011709copy number variation1nstd229human GRCh38 chr20: 5,493,038-5,939,581 , GRCh37.p13 chr20: 5,473,684-5,920,227 LINC00654, EIF4EP1, 9 more genes
    nsv7011702copy number variation1nstd229human GRCh38 chr20: 5,462,243-5,827,773 , GRCh37.p13 chr20: 5,442,889-5,808,419 LINC00654, GPCPD1, 7 more genes
    nsv7010963copy number variation1nstd229human GRCh38 chr20: 5,830,371-5,830,440 , GRCh37.p13 chr20: 5,811,017-5,811,086 SHLD1
    nsv7010724copy number variation1nstd229human GRCh38 chr20: 5,351,177-5,818,572 , GRCh37.p13 chr20: 5,331,823-5,799,218 EIF4EP1, GPCPD1, 8 more genes
    nsv7010044copy number variation1nstd229human GRCh38 chr20: 5,842,288-5,857,235 , GRCh37.p13 chr20: 5,822,934-5,837,881 SHLD1
    nsv7008119copy number variation1nstd229human GRCh38 chr20: 5,783,703-5,783,903 , GRCh37.p13 chr20: 5,764,349-5,764,549 SHLD1
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