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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
    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
    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
    nsv7008728copy number variation1nstd229human GRCh38 chr20: 2,208,621-2,208,807 , GRCh37.p13 chr20: 2,189,267-2,189,453 LINC03086
    nsv7006227copy number variation1nstd229human GRCh38 chr20: 2,169,054-2,208,624 , GRCh37.p13 chr20: 2,149,700-2,189,270 LINC03086, LOC105372502
    nsv7006184copy number variation1nstd229human GRCh38 chr20: 2,201,801-2,205,900 , GRCh37.p13 chr20: 2,182,447-2,186,546 LINC03086, LOC105372502
    nsv7003903copy number variation1nstd229human GRCh38 chr20: 2,189,701-2,214,700 , GRCh37.p13 chr20: 2,170,347-2,195,346 LINC03086, LOC105372502
    nsv6522274copy number variation1nstd223human GRCh38 chr20: 2,202,637-2,205,971 , GRCh37.p13 chr20: 2,183,283-2,186,617 LINC03086
    nsv6134014copy number variation1nstd213human GRCh37 chr20: 2,020,000-2,210,001 , GRCh38.p12 chr20: 2,039,354-2,229,355 RPL7P2, STK35, 2 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5516445copy number variation1nstd206human GRCh38 chr20: 2,202,638-2,205,913 , GRCh37.p13 chr20: 2,183,284-2,186,559 LINC03086
    nsv5025058copy number variation1nstd200human GRCh38 chr20: 2,056,134-2,737,157 , GRCh37.p13 chr20: 2,036,780-2,717,803 , LOC105372507, 22 more genes
    nsv4861643copy number variation1nstd200human GRCh37 chr20: 2,183,258-2,186,589 , GRCh38.p12 chr20: 2,202,612-2,205,943 LINC03086
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
    nsv4630181copy number variation1nstd183human GRCh37 chr20: 2,192,516-2,229,251 , GRCh38.p12 chr20: 2,211,870-2,248,605 LINC03086
    nsv4627448copy number variation1nstd183human GRCh37 chr20: 2,183,227-2,186,521 , GRCh38.p12 chr20: 2,202,581-2,205,875 LINC03086
    nsv4427790copy number variation1nstd174human GRCh37 chr20: 2,183,227-2,186,626 , GRCh38.p12 chr20: 2,202,581-2,205,980 LINC03086
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
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