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Items: 1 to 20 of 104

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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
    nsv7095878copy number variation1nstd102humanUncertain significance GRCh37 chr20: 1,959,939-1,963,730 , GRCh38.p12 chr20: 1,979,293-1,983,084 PDYN-AS1, PDYN
    nsv7074650inversion1nstd229human GRCh38 chr20: 945,543-2,680,685 , GRCh37.p13 chr20: 926,186-2,661,331 , SDCBP2-AS1, 54 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
    nsv7060041inversion1nstd229human GRCh38 chr20: 1,976,025-1,981,486 , GRCh37.p13 chr20: 1,956,671-1,962,132 PDYN-AS1, PDYN
    nsv7059406inversion1nstd229human GRCh38 chr20: 1,739,736-2,068,687 , GRCh37.p13 chr20: 1,720,382-2,049,333 , PDYN-AS1, 6 more genes
    nsv7010923copy number variation1nstd229human GRCh38 chr20: 1,938,612-1,986,344 , GRCh37.p13 chr20: 1,919,258-1,966,990 SIRPA, PDYN, 1 more genes
    nsv7005142copy number variation1nstd229human GRCh38 chr20: 1,991,132-1,991,524 , GRCh37.p13 chr20: 1,971,778-1,972,170 PDYN-AS1, PDYN
    nsv6998989copy number variation1nstd229human GRCh38 chr20: 1,858,021-2,029,126 , GRCh37.p13 chr20: 1,838,667-2,009,772 , PDYN-AS1, 3 more genes
    nsv6310990copy number variation1nstd102humanUncertain significance GRCh37 chr20: 1,960,969-1,963,730 , GRCh38.p12 chr20: 1,980,323-1,983,084 PDYN-AS1, PDYN
    nsv6134274copy number variation1nstd213human GRCh37 chr20: 1,750,000-2,130,001 , GRCh38.p12 chr20: 1,769,354-2,149,355 , PDYN, 7 more genes
    nsv6133904copy number variation1nstd213human GRCh37 chr20: 1-1,970,001 , GRCh38.p12 chr20: 79,361-1,989,355 , CSNK2A1, 57 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5530822copy number variation1nstd206human GRCh38 chr20: 1,976,197-1,977,429 , GRCh37.p13 chr20: 1,956,843-1,958,075 PDYN-AS1, PDYN
    nsv5530086copy number variation1nstd206human GRCh38 chr20: 1,984,049-1,984,107 , GRCh37.p13 chr20: 1,964,695-1,964,753 PDYN-AS1, PDYN
    nsv5525270copy number variation1nstd206human GRCh38 chr20: 1,983,659-1,983,772 , GRCh37.p13 chr20: 1,964,305-1,964,418 PDYN-AS1, PDYN
    nsv4865401copy number variation1nstd200human GRCh37 chr20: 1,956,810-1,958,080 , GRCh38.p12 chr20: 1,976,164-1,977,434 PDYN-AS1, PDYN
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
    nsv4630626copy number variation1nstd183human GRCh37 chr20: 1,387,340-2,110,072 , GRCh38.p12 chr20: 1,406,696-2,129,426 , STK35, 22 more genes
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