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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
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7062382inversion1nstd229human GRCh38 chr20: 2,694,955-2,695,004 , GRCh37.p13 chr20: 2,675,601-2,675,650 EBF4
    nsv7013270copy number variation1nstd229human GRCh38 chr20: 2,710,449-2,721,755 , GRCh37.p13 chr20: 2,691,095-2,702,401 EBF4
    nsv7011978copy number variation1nstd229human GRCh38 chr20: 2,732,401-2,734,600 , GRCh37.p13 chr20: 2,713,047-2,715,246 EBF4
    nsv7011451copy number variation1nstd229human GRCh38 chr20: 2,048,209-2,717,834 , GRCh37.p13 chr20: 2,028,855-2,698,480 SNORD86, TGM3, 21 more genes
    nsv7011319copy number variation1nstd229human GRCh38 chr20: 2,709,330-2,749,718 , GRCh37.p13 chr20: 2,689,976-2,730,364 EBF4
    nsv6999024copy number variation1nstd229human GRCh38 chr20: 2,521,750-2,691,136 , GRCh37.p13 chr20: 2,502,396-2,671,782 NOP56, SNORD86, 12 more genes
    nsv6596575inversion1nstd223human GRCh38 chr20: 2,715,812-2,716,511 , GRCh37.p13 chr20: 2,696,458-2,697,157 EBF4
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6530696copy number variation1nstd223human GRCh38 chr20: 2,696,301-2,697,400 , GRCh37.p13 chr20: 2,676,947-2,678,046 EBF4
    nsv6528627copy number variation1nstd223human GRCh38 chr20: 2,737,170-2,779,572 , GRCh37.p13 chr20: 2,717,816-2,760,218 EBF4, RPL19P1
    nsv6524033copy number variation1nstd223human GRCh38 chr20: 2,737,201-2,737,900 , GRCh37.p13 chr20: 2,717,847-2,718,546 EBF4
    nsv6521850copy number variation1nstd223human GRCh38 chr20: 2,737,123-2,737,838 , GRCh37.p13 chr20: 2,717,769-2,718,484 EBF4
    nsv6516399copy number variation1nstd223human GRCh38 chr20: 2,729,763-2,730,356 , GRCh37.p13 chr20: 2,710,409-2,711,002 EBF4
    nsv6251178mobile element insertion1nstd215human GRCh38 chr20: 2,749,418-2,749,418 , GRCh37.p13 chr20: 2,730,064-2,730,064 EBF4
    nsv6133803copy number variation1nstd213human GRCh37 chr20: 2,720,000-3,420,001 , GRCh38.p12 chr20: 2,739,354-3,439,354 AVP, GNRH2, 26 more genes
    nsv6052065copy number variation1nstd212human GRCh38 chr20: 2,750,466-2,751,109 , GRCh37.p13 chr20: 2,731,112-2,731,755 EBF4
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