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Items: 1 to 20 of 101

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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
    nsv7142561copy number variation1nstd232human GRCh37.p13 chr20: 2,636,157-2,636,238 , GRCh38.p12 chr20: 2,655,511-2,655,592 NOP56, SNORD57, 3 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
    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
    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
    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
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6527105copy number variation1nstd223human GRCh38 chr20: 2,603,189-2,656,563 , GRCh37.p13 chr20: 2,583,835-2,637,209 MIR1292, SNORD110, 8 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5360006translocation1nstd200human GRCh38 chr20: 2,656,549-2,656,549 , GRCh38 chr20: 2,656,781-2,656,781 , GRCh37.p13 chr20: 2,637,195-2,637,195 , GRCh37.p13 chr20: 2,637,427-2,637,427 IDH3B, NOP56, 3 more genes
    nsv5343167translocation1nstd200human GRCh37 chr20: 2,637,195-2,637,195 , GRCh37 chr20: 2,637,428-2,637,428 , GRCh38.p12 chr20: 2,656,782-2,656,782 , GRCh38.p12 chr20: 2,656,549-2,656,549 IDH3B, NOP56, 3 more genes
    nsv5327107translocation1nstd204human GRCh37.p13 chr20: 2,637,541-2,637,541 , GRCh37.p13 chr20: 2,637,727-2,637,727 , GRCh38.p13 chr20: 2,656,895-2,656,895 , GRCh38.p13 chr20: 2,657,081-2,657,081 IDH3B, NOP56, 2 more genes
    nsv5324375translocation1nstd204human GRCh37.p13 chr20: 2,637,195-2,637,195 , GRCh37.p13 chr20: 2,637,427-2,637,427 , GRCh38.p13 chr20: 2,656,549-2,656,549 , GRCh38.p13 chr20: 2,656,781-2,656,781 IDH3B, NOP56, 3 more genes
    nsv5025066copy number variation1nstd200human GRCh38 chr20: 2,603,189-2,656,563 , GRCh37.p13 chr20: 2,583,835-2,637,209 LOC105372505, SNORD110, 8 more genes
    nsv5025058copy number variation1nstd200human GRCh38 chr20: 2,056,134-2,737,157 , GRCh37.p13 chr20: 2,036,780-2,717,803 , LOC105372507, 22 more genes
    nsv4676392copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,412,267-2,644,557 , GRCh38.p12 chr20: 2,431,621-2,663,911 SNORD119, TMC2, 13 more genes
    nsv4422729copy number variation1nstd174human GRCh37 chr20: 2,631,269-2,970,332 , GRCh38.p12 chr20: 2,650,623-2,989,686 , VPS16, 17 more genes
    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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