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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145153insertion1nstd232human GRCh37.p13 chr22: 47,740,747-47,740,747 , GRCh38.p12 chr22: 47,344,997-47,344,997 LOC339685
    nsv7137312insertion1nstd232human GRCh37.p13 chr22: 47,769,362-47,769,362 , GRCh38.p12 chr22: 47,373,612-47,373,612 LOC339685
    nsv7074464inversion1nstd229human GRCh38 chr22: 43,918,591-49,788,574 , GRCh37.p13 chr22: 44,314,471-50,182,222 LOC107985536, LINC02939, 94 more genes
    nsv7071530inversion1nstd229human GRCh38 chr22: 46,297,731-49,136,444 , GRCh37.p13 chr22: 46,693,628-49,532,168 NHIP, GTSE1, 24 more genes
    nsv7063798inversion1nstd229human GRCh38 chr22: 46,184,190-49,118,231 , GRCh37.p13 chr22: 46,580,087-49,513,955 LOC105373080, LOC105373086, 29 more genes
    nsv7037933copy number variation1nstd229human GRCh38 chr22: 47,326,757-47,356,830 , GRCh37.p13 chr22: 47,722,507-47,752,580 LOC339685
    nsv7037710copy number variation1nstd229human GRCh38 chr22: 47,320,364-48,327,600 , GRCh37.p13 chr22: 47,716,114-48,723,412 LOC107985581, LINC01644, 5 more genes
    nsv7037369copy number variation1nstd229human GRCh38 chr22: 47,373,634-47,373,671 , GRCh37.p13 chr22: 47,769,384-47,769,421 LOC339685
    nsv7034046copy number variation1nstd229human GRCh38 chr22: 47,184,701-47,830,000 , GRCh37.p13 chr22: 47,580,452-48,225,749 LOC339685, EPIC1, 3 more genes
    nsv7033672copy number variation1nstd229human GRCh38 chr22: 46,403,349-47,363,632 , GRCh37.p13 chr22: 46,799,246-47,759,382 TBC1D22A-AS1, CELSR1, 8 more genes
    nsv7032364copy number variation1nstd229human GRCh38 chr22: 47,331,287-47,477,357 , GRCh37.p13 chr22: 47,727,037-47,873,106 LOC339685, LINC01644
    nsv7030897copy number variation1nstd229human GRCh38 chr22: 47,341,988-47,352,624 , GRCh37.p13 chr22: 47,737,738-47,748,374 LOC339685
    nsv7029685copy number variation1nstd229human GRCh38 chr22: 47,361,063-47,417,226 , GRCh37.p13 chr22: 47,756,813-47,812,976 LOC339685
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7025283copy number variation1nstd229human GRCh38 chr22: 44,970,256-48,899,837 , GRCh37.p13 chr22: 45,366,136-49,295,649 TAFA5, TRMU, 65 more genes
    nsv7024153copy number variation1nstd229human GRCh38 chr22: 47,372,706-47,382,212 , GRCh37.p13 chr22: 47,768,456-47,777,962 LOC339685
    nsv7023266copy number variation1nstd229human GRCh38 chr22: 47,369,405-47,551,773 , GRCh37.p13 chr22: 47,765,155-47,947,522 LOC339685, LINC01644
    nsv7022630copy number variation1nstd229human GRCh38 chr22: 47,370,467-47,370,614 , GRCh37.p13 chr22: 47,766,217-47,766,364 LOC339685
    nsv6638073copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,436,847-51,188,164 , GRCh38.p12 chr22: 43,040,841-50,749,736 SCUBE1-AS1, MIR6821, 165 more genes
    nsv6637969copy number variation1nstd102humanPathogenic GRCh37 chr22: 44,178,749-51,183,840 , GRCh38.p12 chr22: 43,782,869-50,745,412 LOC105373081, RPL35AP36, 148 more genes
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