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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5164661mobile element insertion1nstd203human GRCh38 chr20: 58,876,922-58,876,936 , GRCh37.p13 chr20: 57,451,977-57,451,991 GNAS, LOC101927932
    nsv5013376copy number variation1nstd200human GRCh38 chr20: 58,866,173-58,868,001 , GRCh37.p13 chr20: 57,441,228-57,443,056 LOC101927932, GNAS
    nsv5013375copy number variation1nstd200human GRCh38 chr20: 58,859,659-58,861,926 , GRCh37.p13 chr20: 57,434,714-57,436,981 GNAS, LOC101927932
    nsv4854052copy number variation1nstd200human GRCh37 chr20: 57,434,714-57,436,981 , GRCh38.p12 chr20: 58,859,659-58,861,926 LOC101927932, GNAS
    nsv4728701copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 57,474,232-57,484,204 , GRCh38 chr20: 58,899,177-58,909,149 GNAS
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4633604copy number variation1nstd183human GRCh37 chr20: 57,464,208-57,465,190 , GRCh38.p12 chr20: 58,889,153-58,890,135 LOC101927932, GNAS
    nsv4632841copy number variation1nstd183human GRCh37 chr20: 57,464,236-57,466,904 , GRCh38.p12 chr20: 58,889,181-58,891,849 GNAS, LOC101927932
    nsv4632753copy number variation1nstd183human GRCh37 chr20: 57,464,179-57,464,421 , GRCh38.p12 chr20: 58,889,124-58,889,366 GNAS, LOC101927932
    nsv4631658copy number variation1nstd183human GRCh37 chr20: 57,466,505-57,466,893 , GRCh38.p12 chr20: 58,891,450-58,891,838 GNAS
    nsv4620803copy number variation2nstd183human GRCh37 chr20: 57,465,451-57,467,183 , GRCh38.p12 chr20: 58,890,396-58,892,128 GNAS
    nsv4561990insertion1nstd166human GRCh37.p13 chr20: 57,438,855-57,438,855 , GRCh38.p12 chr20: 58,863,800-58,863,800 LOC101927932, GNAS
    nsv4511294mobile element insertion1nstd166human GRCh37.p13 chr20: 57,458,635-57,458,635 , GRCh38.p12 chr20: 58,883,580-58,883,580 LOC101927932, GNAS
    nsv4504886mobile element insertion1nstd166human GRCh37.p13 chr20: 57,432,069-57,432,069 , GRCh38.p12 chr20: 58,857,014-58,857,014 GNAS
    nsv4422988copy number variation1nstd174human GRCh37 chr20: 57,465,278-57,467,183 , GRCh38.p12 chr20: 58,890,223-58,892,128 GNAS
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4291505copy number variation1nstd166human GRCh37.p13 chr20: 57,441,228-57,443,056 , GRCh38.p12 chr20: 58,866,173-58,868,001 GNAS, LOC101927932
    nsv4280586copy number variation1nstd166human GRCh37.p13 chr20: 57,434,715-57,436,981 , GRCh38.p12 chr20: 58,859,660-58,861,926 GNAS, LOC101927932
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