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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072579inversion1nstd229human GRCh38 chr22: 42,823,959-42,828,557 , GRCh37.p13 chr22: 43,219,965-43,224,563 ARFGAP3
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7035525copy number variation1nstd229human GRCh38 chr22: 42,798,233-42,889,760 , GRCh37.p13 chr22: 43,194,239-43,285,766 ARFGAP3, LOC692246, 2 more genes
    nsv7035047copy number variation1nstd229human GRCh38 chr22: 42,836,324-42,838,869 , GRCh37.p13 chr22: 43,232,330-43,234,875 ARFGAP3
    nsv7033765copy number variation1nstd229human GRCh38 chr22: 42,637,604-42,869,737 , GRCh37.p13 chr22: 43,033,610-43,265,743 PACSIN2, GOLGA2P4, 9 more genes
    nsv7033177copy number variation1nstd229human GRCh38 chr22: 42,798,273-42,798,454 , GRCh37.p13 chr22: 43,194,279-43,194,460 ARFGAP3
    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
    nsv7025972copy number variation1nstd229human GRCh38 chr22: 42,795,221-42,880,516 , GRCh37.p13 chr22: 43,191,227-43,276,522 LOC101927393, LOC692246, 2 more genes
    nsv7023568copy number variation1nstd229human GRCh38 chr22: 42,856,901-42,920,600 , GRCh37.p13 chr22: 43,252,907-43,316,606 LOC101927393, PACSIN2, 1 more genes
    nsv7022423copy number variation1nstd229human GRCh38 chr22: 42,791,901-42,833,400 , GRCh37.p13 chr22: 43,187,907-43,229,406 ARFGAP3, LOC100422416
    nsv7021742copy number variation1nstd229human GRCh38 chr22: 42,779,701-42,986,800 , GRCh37.p13 chr22: 43,175,707-43,382,806 LOC101927393, LOC692246, 5 more genes
    nsv7020901copy number variation1nstd229human GRCh38 chr22: 42,792,501-42,794,700 , GRCh37.p13 chr22: 43,188,507-43,190,706 ARFGAP3, LOC100422416
    nsv7018150copy number variation1nstd229human GRCh38 chr22: 42,835,311-42,871,628 , GRCh37.p13 chr22: 43,231,317-43,267,634 LOC101927393, ARFGAP3, 2 more genes
    nsv6597126inversion1nstd223human GRCh38 chr22: 42,837,344-42,837,773 , GRCh37.p13 chr22: 43,233,350-43,233,779 ARFGAP3
    nsv6595866inversion1nstd223human GRCh38 chr22: 42,837,462-42,837,869 , GRCh37.p13 chr22: 43,233,468-43,233,875 ARFGAP3
    nsv6542967copy number variation1nstd223human GRCh38 chr22: 42,831,179-42,832,423 , GRCh37.p13 chr22: 43,227,185-43,228,429 ARFGAP3
    nsv6541080copy number variation1nstd223human GRCh38 chr22: 42,856,601-42,858,900 , GRCh37.p13 chr22: 43,252,607-43,254,906 ARFGAP3
    nsv6540741copy number variation1nstd223human GRCh38 chr22: 42,775,960-42,810,225 , GRCh37.p13 chr22: 43,171,966-43,206,231 LOC100422416, GOLGA2P4, 3 more genes
    nsv6535893copy number variation1nstd223human GRCh38 chr22: 41,572,303-44,198,988 , GRCh37.p13 chr22: 41,968,307-44,594,868 , RPS25P10, 87 more genes
    nsv6315490copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,103,054-43,207,442 , GRCh38.p12 chr22: 42,707,048-42,811,436 ARFGAP3, A4GALT, 4 more genes
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