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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7146380copy number variation1nstd232human GRCh37.p13 chr20: 57,478,640-57,478,725 , GRCh38.p12 chr20: 58,903,585-58,903,670 GNAS
    nsv7145907insertion1nstd232human GRCh37.p13 chr20: 57,478,849-57,478,849 , GRCh38.p12 chr20: 58,903,794-58,903,794 GNAS
    nsv7144753insertion1nstd232human GRCh37.p13 chr20: 57,478,846-57,478,846 , GRCh38.p12 chr20: 58,903,791-58,903,791 GNAS
    nsv7142509insertion1nstd232human GRCh37.p13 chr20: 57,480,537-57,480,537 , GRCh38.p12 chr20: 58,905,482-58,905,482 GNAS
    nsv7141736copy number variation1nstd232human GRCh37.p13 chr20: 57,484,478-57,484,574 , GRCh38.p12 chr20: 58,909,423-58,909,519 GNAS
    nsv7137318insertion1nstd232human GRCh37.p13 chr20: 57,466,921-57,466,921 , GRCh38.p12 chr20: 58,891,866-58,891,866 GNAS
    nsv7095908copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,478,707-57,478,866 , GRCh38.p12 chr20: 58,903,652-58,903,811 GNAS
    nsv7095907copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,466,782-57,485,884 , GRCh38.p12 chr20: 58,891,727-58,910,829 GNAS
    nsv7095906copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr20: 57,466,782-57,466,940 , GRCh38.p12 chr20: 58,891,727-58,891,885 GNAS
    nsv7095799copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,485,079-57,487,993 , GRCh38.p12 chr20: 58,910,024-58,912,938 GNAS
    nsv7075585inversion1nstd229human GRCh38 chr20: 58,909,933-58,910,056 , GRCh37.p13 chr20: 57,484,988-57,485,111 GNAS
    nsv7073102inversion1nstd229human GRCh38 chr20: 58,529,050-58,860,387 , GRCh37.p13 chr20: 57,104,106-57,435,442 NPEPL1, MIR298, 10 more genes
    nsv7060906inversion1nstd229human GRCh38 chr20: 58,890,226-58,890,336 , GRCh37.p13 chr20: 57,465,281-57,465,391 GNAS
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7033189copy number variation1nstd229human GRCh38 chr20: 58,839,201-58,842,700 , GRCh37.p13 chr20: 57,414,256-57,417,755 GNAS, GNAS-AS1
    nsv7032834copy number variation1nstd229human GRCh38 chr20: 58,901,524-59,002,068 , GRCh37.p13 chr20: 57,476,579-57,577,123 CTSZ, LOC107985382, 3 more genes
    nsv7030666copy number variation1nstd229human GRCh38 chr20: 58,903,792-58,909,345 , GRCh37.p13 chr20: 57,478,847-57,484,400 GNAS
    nsv7028767copy number variation1nstd229human GRCh38 chr20: 58,889,270-58,889,313 , GRCh37.p13 chr20: 57,464,325-57,464,368 LOC101927932, GNAS
    nsv7024508copy number variation1nstd229human GRCh38 chr20: 58,888,301-58,899,700 , GRCh37.p13 chr20: 57,463,356-57,474,755 GNAS, LOC101927932
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