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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
    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
    nsv7017423copy number variation1nstd229human GRCh38 chr20: 2,622,401-2,634,800 , GRCh37.p13 chr20: 2,603,047-2,615,446 LOC105372505, TMC2
    nsv7016237copy number variation1nstd229human GRCh38 chr20: 2,634,055-2,638,677 , GRCh37.p13 chr20: 2,614,701-2,619,323 TMC2, LOC105372505
    nsv7013493copy number variation1nstd229human GRCh38 chr20: 2,616,844-2,625,211 , GRCh37.p13 chr20: 2,597,490-2,605,857 LOC105372505, TMC2
    nsv7011542copy number variation1nstd229human GRCh38 chr20: 2,347,591-2,615,813 , GRCh37.p13 chr20: 2,328,237-2,596,459 TGM6, LOC105372505, 5 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
    nsv7009460copy number variation1nstd229human GRCh38 chr20: 2,632,089-2,636,365 , GRCh37.p13 chr20: 2,612,735-2,617,011 LOC105372505, TMC2
    nsv7009413copy number variation1nstd229human GRCh38 chr20: 2,624,220-2,630,581 , GRCh37.p13 chr20: 2,604,866-2,611,227 TMC2, LOC105372505
    nsv6999656copy number variation1nstd229human GRCh38 chr20: 2,618,491-2,652,515 , GRCh37.p13 chr20: 2,599,137-2,633,161 TMC2, NOP56, 3 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
    nsv6998629copy number variation1nstd229human GRCh38 chr20: 2,642,732-2,645,231 , GRCh37.p13 chr20: 2,623,378-2,625,877 LOC105372505
    nsv6626337copy number variation1nstd224human GRCh37 chr20: 2,605,044-2,632,010 , GRCh38.p12 chr20: 2,624,398-2,651,364 LOC105372505, NOP56, 2 more genes
    nsv6599060inversion1nstd223human GRCh38 chr20: 2,638,065-2,639,188 , GRCh37.p13 chr20: 2,618,711-2,619,834 LOC105372505, TMC2
    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
    nsv6520631copy number variation1nstd223human GRCh38 chr20: 2,642,732-2,645,229 , GRCh37.p13 chr20: 2,623,378-2,625,875 LOC105372505
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