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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
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 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
    nsv7095551copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,063,276-3,903,941 , GRCh38.p12 chr20: 3,082,630-3,923,294 PANK2, MAVS, 31 more genes
    nsv7074742inversion1nstd229human GRCh38 chr20: 3,441,683-5,027,331 , GRCh37.p13 chr20: 3,422,330-5,007,977 MAVS, MIR103B2, 33 more genes
    nsv7074666inversion1nstd229human GRCh38 chr20: 3,679,053-3,691,775 , GRCh37.p13 chr20: 3,659,700-3,672,422 SIGLEC1, ADAM33
    nsv7074584inversion1nstd229human GRCh38 chr20: 3,680,232-3,680,375 , GRCh37.p13 chr20: 3,660,879-3,661,022 ADAM33
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7073754inversion1nstd229human GRCh38 chr20: 3,665,621-3,701,066 , GRCh37.p13 chr20: 3,646,268-3,681,713 SIGLEC1, ADAM33
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7017327copy number variation1nstd229human GRCh38 chr20: 3,655,955-3,680,084 , GRCh37.p13 chr20: 3,636,602-3,660,731 GFRA4, ADAM33
    nsv7015272copy number variation1nstd229human GRCh38 chr20: 3,519,388-3,799,972 , GRCh37.p13 chr20: 3,500,035-3,780,619 CDC25B, HSPA12B, 7 more genes
    nsv7014246copy number variation1nstd229human GRCh38 chr20: 3,667,833-3,667,893 , GRCh37.p13 chr20: 3,648,480-3,648,540 ADAM33
    nsv7014160copy number variation1nstd229human GRCh38 chr20: 3,658,736-3,725,888 , GRCh37.p13 chr20: 3,639,383-3,706,535 GFRA4, ADAM33, 1 more genes
    nsv7013299copy number variation1nstd229human GRCh38 chr20: 3,674,301-3,677,800 , GRCh37.p13 chr20: 3,654,948-3,658,447 ADAM33
    nsv7007813copy number variation1nstd229human GRCh38 chr20: 3,543,154-3,905,714 , GRCh37.p13 chr20: 3,523,801-3,886,361 LINC01730, HSPA12B, 12 more genes
    nsv7005642copy number variation1nstd229human GRCh38 chr20: 3,652,051-3,683,239 , GRCh37.p13 chr20: 3,632,698-3,663,886 GFRA4, ADAM33
    nsv7004822copy number variation1nstd229human GRCh38 chr20: 3,680,875-3,680,921 , GRCh37.p13 chr20: 3,661,522-3,661,568 ADAM33
    nsv7001931copy number variation1nstd229human GRCh38 chr20: 3,676,065-3,694,273 , GRCh37.p13 chr20: 3,656,712-3,674,920 ADAM33, SIGLEC1
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