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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
    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
    nsv7060985inversion1nstd229human GRCh38 chr20: 2,809,464-3,136,537 , GRCh37.p13 chr20: 2,790,110-3,117,183 GNRH2, LOC101929098, 11 more genes
    nsv7004186copy number variation1nstd229human GRCh38 chr20: 2,806,375-2,847,964 , GRCh37.p13 chr20: 2,787,021-2,828,610 C20orf141, VPS16, 2 more genes
    nsv6626559copy number variation1nstd224human GRCh37 chr20: 2,796,081-3,070,571 , GRCh38.p12 chr20: 2,815,435-3,089,925 PTPRA, MRPS26, 8 more genes
    nsv6599489inversion1nstd223human GRCh38 chr20: 2,809,549-3,136,794 , GRCh37.p13 chr20: 2,790,195-3,117,440 AVP, GNRH2, 11 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
    nsv6133803copy number variation1nstd213human GRCh37 chr20: 2,720,000-3,420,001 , GRCh38.p12 chr20: 2,739,354-3,439,354 AVP, GNRH2, 26 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv4457667copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,738,670-3,054,217 , GRCh38.p12 chr20: 2,758,024-3,073,571 CPXM1, RPL19P1, 10 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
    nsv4330625inversion1nstd166human GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660 , ADRA1D, 89 more genes
    nsv3968363copy number variation1nstd168human GRCh38 chr20: 2,793,342-2,844,769 , GRCh37.p13 chr20: 2,773,988-2,825,415 VPS16, CPXM1, 3 more genes
    nsv3923490copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049 LINC01751, RNA5SP474, 238 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3922038copy number variation1nstd102humanUncertain significance GRCh38 chr20: 80,927-5,447,679 , NCBI36 chr20: 9,568-5,376,325 , GRCh37 chr20: 61,568-5,428,325 LOC105372509, SIRPD, 150 more genes
    nsv3921981copy number variation1nstd102humanUncertain significance GRCh38 chr20: 2,595,077-3,004,837 , NCBI36 chr20: 2,523,723-2,933,483 , GRCh37 chr20: 2,575,723-2,985,483 IDH3B, TMEM239, 17 more genes
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