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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142511copy number variation1nstd232human GRCh37.p13 chr22: 47,083,172-47,083,234 , GRCh38.p12 chr22: 46,687,275-46,687,337 CERK
    nsv7074464inversion1nstd229human GRCh38 chr22: 43,918,591-49,788,574 , GRCh37.p13 chr22: 44,314,471-50,182,222 LOC107985536, LINC02939, 94 more genes
    nsv7071552inversion1nstd229human GRCh38 chr22: 46,714,677-46,785,916 , GRCh37.p13 chr22: 47,110,574-47,181,813 CERK, TBC1D22A, 1 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
    nsv7069889inversion1nstd229human GRCh38 chr22: 46,693,920-46,722,841 , GRCh37.p13 chr22: 47,089,817-47,118,738 CERK
    nsv7063798inversion1nstd229human GRCh38 chr22: 46,184,190-49,118,231 , GRCh37.p13 chr22: 46,580,087-49,513,955 LOC105373080, LOC105373086, 29 more genes
    nsv7037233copy number variation1nstd229human GRCh38 chr22: 46,658,457-46,876,956 , GRCh37.p13 chr22: 47,054,354-47,272,852 GRAMD4, TBC1D22A, 2 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
    nsv7033473copy number variation1nstd229human GRCh38 chr22: 46,731,686-46,741,107 , GRCh37.p13 chr22: 47,127,583-47,137,004 LOC105373077, CERK
    nsv7033271copy number variation1nstd229human GRCh38 chr22: 46,700,698-46,704,811 , GRCh37.p13 chr22: 47,096,595-47,100,708 CERK
    nsv7030562copy number variation1nstd229human GRCh38 chr22: 46,681,930-46,696,645 , GRCh37.p13 chr22: 47,077,827-47,092,542 GRAMD4, CERK
    nsv7029735copy number variation1nstd229human GRCh38 chr22: 46,692,690-46,697,279 , GRCh37.p13 chr22: 47,088,587-47,093,176 CERK
    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
    nsv7027379copy number variation1nstd229human GRCh38 chr22: 46,713,687-46,719,412 , GRCh37.p13 chr22: 47,109,584-47,115,309 CERK
    nsv7026446copy number variation1nstd229human GRCh38 chr22: 46,689,439-46,703,399 , GRCh37.p13 chr22: 47,085,336-47,099,296 CERK
    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
    nsv7024083copy number variation1nstd229human GRCh38 chr22: 46,722,022-46,727,888 , GRCh37.p13 chr22: 47,117,919-47,123,785 CERK
    nsv7021561copy number variation1nstd229human GRCh38 chr22: 46,724,301-46,730,800 , GRCh37.p13 chr22: 47,120,198-47,126,697 CERK
    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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