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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972786insertion1nstd209human GRCh38 chr22: 35,075,643-35,075,643 , GRCh37.p13 chr22: 35,471,636-35,471,636 ISX
    nsv5955026copy number variation1nstd209human GRCh38 chr22: 35,071,097-35,071,167 , GRCh37.p13 chr22: 35,467,090-35,467,160 ISX
    nsv5535078copy number variation1nstd206human GRCh38 chr22: 35,064,783-35,171,588 , GRCh37.p13 chr22: 35,460,776-35,567,581 ISX, LINC01399
    nsv5037085copy number variation1nstd200human GRCh38 chr22: 35,063,120-35,067,105 , GRCh37.p13 chr22: 35,459,113-35,463,098 ISX
    nsv5033747copy number variation1nstd200human GRCh38 chr22: 35,080,867-35,086,911 , GRCh37.p13 chr22: 35,476,860-35,482,904 ISX
    nsv4886510copy number variation1nstd200human GRCh37 chr22: 35,459,113-35,463,098 , GRCh38.p12 chr22: 35,063,120-35,067,105 ISX
    nsv4736828copy number variation1nstd199human GRCh37 chr22: 35,460,250-35,460,565 , GRCh38.p12 chr22: 35,064,257-35,064,572 ISX
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4634140copy number variation1nstd183human GRCh37 chr22: 35,460,776-35,567,582 , GRCh38.p12 chr22: 35,064,783-35,171,589 LINC01399, ISX
    nsv4631526copy number variation1nstd183human GRCh37 chr22: 35,469,747-35,471,058 , GRCh38.p12 chr22: 35,073,754-35,075,065 ISX
    nsv4628603copy number variation1nstd183human GRCh37 chr22: 35,469,747-35,471,007 , GRCh38.p12 chr22: 35,073,754-35,075,014 ISX
    nsv4622926copy number variation1nstd183human GRCh37 chr22: 35,458,059-35,469,591 , GRCh38.p12 chr22: 35,062,066-35,073,598 ISX
    nsv4622771copy number variation1nstd183human GRCh37 chr22: 34,835,597-35,485,775 , GRCh38.p12 chr22: 34,439,606-35,089,782 , ISX, 5 more genes
    nsv4501198mobile element insertion1nstd166human GRCh37.p13 chr22: 35,471,621-35,471,621 , GRCh38.p12 chr22: 35,075,628-35,075,628 ISX
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4289512copy number variation1nstd166human GRCh37.p13 chr22: 35,463,157-35,465,283 , GRCh38.p12 chr22: 35,067,164-35,069,290 ISX
    nsv4289064copy number variation1nstd166human GRCh37.p13 chr22: 35,460,776-35,567,581 , GRCh38.p12 chr22: 35,064,783-35,171,588 LINC01399, ISX
    nsv4283011copy number variation1nstd166human GRCh37.p13 chr22: 35,432,737-35,478,937 , GRCh38.p12 chr22: 35,036,745-35,082,944 ISX
    nsv4279568copy number variation1nstd166human GRCh37.p13 chr22: 35,450,715-35,462,165 , GRCh38.p12 chr22: 35,054,722-35,066,172 ISX
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