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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4330625inversion1nstd166human GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660 , ADRA1D, 89 more genes
    nsv4270033copy number variation1nstd166human GRCh37.p13 chr20: 2,636,860-2,637,723 , GRCh38.p12 chr20: 2,656,214-2,657,077 IDH3B, SNORD56, 3 more genes
    nsv4258983copy number variation1nstd166human GRCh37.p13 chr20: 2,637,195-2,637,418 , GRCh38.p12 chr20: 2,656,549-2,656,772 SNORD57, SNORD86, 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
    nsv3921972copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923 PTMAP3, LOC105372517, 331 more genes
    nsv3920692copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,507,401-3,062,297 , NCBI36 chr20: 2,455,401-3,010,297 , GRCh38 chr20: 2,526,755-3,081,651 TMC2, MRPS26, 23 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
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