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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148270copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,838-20,508,931 , GRCh38.p12 chr22: 18,483,514-20,345,217 DGCR2, MIR4761, 79 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
    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
    nsv7095928copy number variation2nstd102humanPathogenic GRCh37 chr22: 17,565,982-20,052,185 , GRCh38.p12 chr22: 17,085,092-20,064,662 CA15P1, BID, 103 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
    nsv6638022copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,916,843-21,075,592 , GRCh38.p12 chr22: 18,339,130-20,721,304 FAM230J, LOC107985588, 107 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
    nsv6637960copy number variation1nstd102humanPathogenic GRCh37 chr22: 19,046,677-21,465,662 , GRCh38.p12 chr22: 18,339,130-21,111,373 TSSK2, LOC112268297, 125 more genes
    nsv6637923copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-18,916,828 , GRCh38.p12 chr22: 16,408,174-18,929,315 ANKRD62P1, IGKV1OR22-1, 87 more genes
    nsv6637871copy number variation1nstd102humanPathogenic GRCh37 chr22: 19,647,905-21,153,690 , GRCh38.p12 chr22: 18,339,130-20,799,402 GGTLC5P, C22orf39, 108 more genes
    nsv6637775copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,916,843-21,798,907 , GRCh38.p12 chr22: 18,339,130-21,444,618 CRKL, E2F6P3, 139 more genes
    nsv6637764copy number variation1nstd102humanUncertain significance GRCh37 chr22: 18,560,247-18,916,828 , GRCh38.p12 chr22: 18,077,481-18,929,315 LOC101060852, FAM230J, 30 more genes
    nsv6637709copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,648,867-21,798,907 , GRCh38.p12 chr22: 18,166,100-21,444,618 FAM230A, GSC2, 144 more genes
    nsv6637680copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,916,828-21,800,797 , GRCh38.p12 chr22: 18,339,130-21,446,508 ABHD17AP4, E2F6P3, 139 more genes
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