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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148280copy number variation1nstd102humanPathogenic GRCh38 chr22: 18,985,739-21,081,116 , GRCh37.p13 chr22: 18,973,252-21,435,405 SLC9A3P2, RNU6-225P, 99 more genes
    nsv7148246copy number variation2nstd102humanPathogenic GRCh37 chr22: 18,893,838-21,416,074 , GRCh38.p12 chr22: 18,339,130-21,061,785 ZDHHC8, FAM230E, 121 more genes
    nsv7148214copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,609,932-21,576,553 , GRCh38.p12 chr22: 18,339,630-21,222,264 IGLL4P, LOC107985584, 129 more genes
    nsv7137150copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,888-21,481,925 , GRCh38.p12 chr22: 18,339,130-21,127,636 LOC107985584, LINC00896, 125 more genes
    nsv7098940copy number variation1nstd102humanUncertain significance GRCh38 chr22: 20,354,589-21,405,291 , GRCh37.p13 chr22: 20,708,879-21,759,580 FAM230B, POM121L7P, 52 more genes
    nsv7098862copy number variation1nstd102humanPathogenic GRCh38 chr22: 18,206,749-21,234,326 , GRCh37.p13 chr22: 18,689,516-21,588,615 GP1BB, IGLL4P, 132 more genes
    nsv7098756copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,886-21,386,103 , GRCh38.p12 chr22: 18,339,130-21,031,814 CCDC188, MED15, 118 more genes
    nsv7095817copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,348,827-21,351,637 , GRCh38.p12 chr22: 20,994,538-20,997,348 LZTR1, THAP7
    nsv7093440copy number variation1nstd102humannot provided GRCh37 chr22: 21,119,379-21,443,283 , GRCh38.p12 chr22: 20,765,091-21,088,994 LZTR1, THAP7-AS1, 15 more genes
    nsv7093409copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,888-21,570,386 , GRCh38.p12 chr22: 18,339,130-21,216,097 FAM247A, P2RX6P, 129 more genes
    nsv7093403copy number variation1nstd102humanPathogenic GRCh37 chr22: 19,184,000-21,416,024 , GRCh38.p12 chr22: 18,339,130-21,061,735 LOC105372862, RPL7AP70, 121 more genes
    nsv7093402copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,894,078-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528 LOC100420103, P2RX6P, 121 more genes
    nsv7093382copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,834,445-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528 DGCR8, SEPTIN5, 121 more genes
    nsv7037518copy number variation1nstd229human GRCh38 chr22: 20,688,140-21,128,714 , GRCh37.p13 chr22: 21,042,428-21,483,003 SERPIND1, SLC7A4, 21 more genes
    nsv7031187copy number variation1nstd229human GRCh38 chr22: 20,991,417-21,032,616 , GRCh37.p13 chr22: 21,345,706-21,386,905 SLC7A4, LZTR1, 5 more genes
    nsv7029274copy number variation1nstd229human GRCh38 chr22: 20,988,206-20,993,420 , GRCh37.p13 chr22: 21,342,495-21,347,709 LZTR1
    nsv7022769copy number variation1nstd229human GRCh38 chr22: 20,994,210-21,015,338 , GRCh37.p13 chr22: 21,348,499-21,369,627 THAP7, TUBA3FP, 3 more genes
    nsv7020265copy number variation1nstd229human GRCh38 chr22: 20,970,601-21,004,300 , GRCh37.p13 chr22: 21,324,890-21,358,589 LZTR1, THAP7-AS1, 2 more genes
    nsv6638009copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,648,867-21,465,659 , GRCh38.p12 chr22: 18,166,100-21,111,370 KLHL22, THAP7-AS1, 130 more genes
    nsv6637971copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,728,957-21,798,907 , GRCh38.p12 chr22: 20,374,667-21,444,618 THAP7-AS1, KLHL22, 53 more genes
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