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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
    nsv7146144copy number variation1nstd232human GRCh37.p13 chr20: 8,551,260-8,551,343 , GRCh38.p12 chr20: 8,570,613-8,570,696 PLCB1
    nsv7142045copy number variation1nstd232human GRCh37.p13 chr20: 8,474,524-8,474,677 , GRCh38.p12 chr20: 8,493,877-8,494,030 PLCB1
    nsv7096275copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,113,299-8,352,117 , GRCh38.p12 chr20: 8,132,652-8,371,470 PLCB1, PLCB1-IT1
    nsv7096088copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,608,921-8,862,496 , GRCh38.p12 chr20: 8,628,274-8,881,849 LOC105372521, RNU105B, 1 more genes
    nsv7095807copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,696,891-8,698,515 , GRCh38.p12 chr20: 8,716,244-8,717,868 PLCB1
    nsv7077635inversion1nstd229human GRCh38 chr20: 8,775,820-8,775,856 , GRCh37.p13 chr20: 8,756,467-8,756,503 PLCB1
    nsv7076963inversion1nstd229human GRCh38 chr20: 8,336,633-8,336,668 , GRCh37.p13 chr20: 8,317,280-8,317,315 PLCB1
    nsv7075121inversion1nstd229human GRCh38 chr20: 8,466,575-8,470,919 , GRCh37.p13 chr20: 8,447,222-8,451,566 PLCB1
    nsv7074525inversion1nstd229human GRCh38 chr20: 8,587,986-8,588,091 , GRCh37.p13 chr20: 8,568,633-8,568,738 PLCB1
    nsv7074519inversion1nstd229human GRCh38 chr20: 8,811,300-8,814,395 , GRCh37.p13 chr20: 8,791,947-8,795,042 PLCB1
    nsv7071893inversion1nstd229human GRCh38 chr20: 8,468,237-8,475,646 , GRCh37.p13 chr20: 8,448,884-8,456,293 PLCB1
    nsv7071854inversion1nstd229human GRCh38 chr20: 8,154,005-8,154,060 , GRCh37.p13 chr20: 8,134,652-8,134,707 PLCB1
    nsv7064436inversion1nstd229human GRCh38 chr20: 8,459,658-8,469,562 , GRCh37.p13 chr20: 8,440,305-8,450,209 PLCB1
    nsv7064038inversion1nstd229human GRCh38 chr20: 8,697,351-8,705,889 , GRCh37.p13 chr20: 8,677,998-8,686,536 PLCB1
    nsv7063767inversion1nstd229human GRCh38 chr20: 8,474,414-8,480,949 , GRCh37.p13 chr20: 8,455,061-8,461,596 PLCB1
    nsv7061818inversion1nstd229human GRCh38 chr20: 7,416,632-9,615,935 , GRCh37.p13 chr20: 7,397,279-9,596,582 RNU105B, RN7SL547P, 15 more genes
    nsv7037978copy number variation1nstd229human GRCh38 chr20: 8,630,680-8,633,947 , GRCh37.p13 chr20: 8,611,327-8,614,594 PLCB1, LOC105372521
    nsv7037839copy number variation1nstd229human GRCh38 chr20: 8,697,847-8,699,678 , GRCh37.p13 chr20: 8,678,494-8,680,325 PLCB1
    nsv7037718copy number variation1nstd229human GRCh38 chr20: 8,876,065-8,876,237 , GRCh37.p13 chr20: 8,856,712-8,856,884 PLCB1
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