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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5729050mobile element insertion1nstd211human GRCh38 chr20: 3,687,446-3,687,446 , GRCh37.p13 chr20: 3,668,093-3,668,093 SIGLEC1
    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
    nsv5526727copy number variation1nstd206human GRCh38 chr20: 3,688,104-3,688,285 , GRCh37.p13 chr20: 3,668,751-3,668,932 SIGLEC1
    nsv5518313copy number variation1nstd206human GRCh38 chr20: 3,686,667-3,687,285 , GRCh37.p13 chr20: 3,667,314-3,667,932 SIGLEC1
    nsv5033561inversion1nstd200human GRCh38 chr20: 3,693,712-5,966,244 , GRCh37.p13 chr20: 3,674,359-5,946,890 , LOC107985411, 53 more genes
    nsv5025080copy number variation1nstd200human GRCh38 chr20: 3,699,790-3,700,785 , GRCh37.p13 chr20: 3,680,437-3,681,432 SIGLEC1
    nsv5025079copy number variation1nstd200human GRCh38 chr20: 3,676,065-3,694,276 , GRCh37.p13 chr20: 3,656,712-3,674,923 SIGLEC1, ADAM33
    nsv5012227copy number variation1nstd200human GRCh38 chr20: 3,688,104-3,688,285 , GRCh37.p13 chr20: 3,668,751-3,668,932 SIGLEC1
    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
    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
    nsv4575671mobile element insertion1nstd166human GRCh37.p13 chr20: 3,668,082-3,668,082 , GRCh38.p12 chr20: 3,687,435-3,687,435 SIGLEC1
    nsv4457744copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,654,723-3,796,884 , GRCh38.p12 chr20: 3,674,076-3,816,237 ADISSP, SPEF1, 6 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
    nsv4270354copy number variation1nstd166human GRCh37.p13 chr20: 3,680,463-3,681,377 , GRCh38.p12 chr20: 3,699,816-3,700,730 SIGLEC1
    nsv4261664copy number variation1nstd166human GRCh37.p13 chr20: 3,668,751-3,668,932 , GRCh38.p12 chr20: 3,688,104-3,688,285 SIGLEC1
    nsv4261064copy number variation1nstd166human GRCh37.p13 chr20: 3,656,712-3,674,920 , GRCh38.p12 chr20: 3,676,065-3,694,273 SIGLEC1, ADAM33
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