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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564166copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,190,178-3,903,961 , GRCh38.p12 chr20: 3,209,532-3,923,314 ADAM33, AP5S1, 23 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv4729952copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,116,478-4,199,486 , GRCh38.p12 chr20: 3,135,832-4,218,839 LOC105372508, CDC25B, 35 more genes
    nsv4729947copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,092,739-4,939,933 , GRCh38.p12 chr20: 3,112,093-4,959,287 SF3A3P1, PRND, 46 more genes
    nsv4729753copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,802,218-4,010,802 , GRCh38.p12 chr20: 2,821,572-4,030,155 DDRGK1, LZTS3, 40 more genes
    nsv4676304copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,246,941-3,514,037 , GRCh38.p12 chr20: 3,266,295-3,533,390 SF3A3P1, LOC105372508, 6 more genes
    nsv4676134copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,806,498-4,007,381 , GRCh38.p12 chr20: 2,825,852-4,026,734 MIR103B2, OXT, 40 more genes
    nsv4626453copy number variation1nstd183human GRCh37 chr20: 3,020,553-3,350,814 , GRCh38.p12 chr20: 3,039,907-3,370,167 DDRGK1, FASTKD5, 16 more genes
    nsv4450870copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,190,178-3,604,448 , GRCh38.p12 chr20: 3,209,532-3,623,801 SF3A3P1, ITPA, 8 more genes
    nsv4417768copy number variation1nstd174human GRCh37 chr20: 3,011,188-3,385,073 , GRCh38.p12 chr20: 3,030,542-3,404,426 LZTS3, UBOX5, 17 more genes
    nsv4377839copy number variation1nstd173human GRCh37 chr20: 3,321,335-3,481,742 , GRCh38.p12 chr20: 3,340,688-3,501,095 LOC105372508, RNU6-1019P, 5 more genes
    nsv4370614copy number variation1nstd173human GRCh37 chr20: 3,321,335-3,481,730 , GRCh38.p12 chr20: 3,340,688-3,501,083 DNAAF9, SF3A3P1, 5 more genes
    nsv4366856copy number variation1nstd173human GRCh37 chr20: 3,321,335-3,497,132 , GRCh38.p12 chr20: 3,340,688-3,516,485 RNU6-1019P, DNAAF9, 5 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
    nsv4272324copy number variation1nstd166human GRCh37.p13 chr20: 3,322,015-3,349,309 , GRCh38.p12 chr20: 3,341,368-3,368,662 DNAAF9, UBE2V1P1, 1 more genes
    nsv4265428copy number variation1nstd166human GRCh37.p13 chr20: 3,208,068-3,394,315 , GRCh38.p12 chr20: 3,227,422-3,413,668 ITPA, DNAAF9, 4 more genes
    nsv4252563copy number variation1nstd166human GRCh37.p13 chr20: 3,340,587-3,340,680 , GRCh38.p12 chr20: 3,359,940-3,360,033 RNU6-1019P, DNAAF9, 1 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
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