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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5368001translocation1nstd200human GRCh38 chr18: 74,158,785-74,158,785 , GRCh38 chr5: 4,687,983-4,687,983 , GRCh37.p13 chr18: 71,826,020-71,826,020 , GRCh37.p13 chr5: 4,688,096-4,688,096 TIMM21
    nsv5024403copy number variation1nstd200human GRCh38 chr18: 73,754,395-74,187,997 , GRCh37.p13 chr18: 71,421,630-71,855,232 TIMM21, LOC105372191, 1 more genes
    nsv5024393copy number variation1nstd200human GRCh38 chr18: 72,896,464-74,189,719 , GRCh37.p13 chr18: 70,563,699-71,856,954 LINC02582, LOC105372191, 5 more genes
    nsv4729869copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 63,747,519-78,014,123 , GRCh38.p12 chr18: 66,080,283-80,256,240 CYB5A, GALR1, 147 more genes
    nsv4729851copy number variation1nstd102humanPathogenic GRCh37 chr18: 70,835,154-78,014,123 , GRCh38.p12 chr18: 73,167,919-80,256,240 ZNF236-DT, LOC339298, 89 more genes
    nsv4676384copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,247,046-78,014,123 , GRCh38.p12 chr18: 65,579,810-80,256,240 LINC02582, LINC01912, 149 more genes
    nsv4676378copy number variation1nstd102humanPathogenic GRCh37 chr18: 56,750,525-78,014,123 , GRCh38.p12 chr18: 59,083,293-80,256,240 HSBP1L1, TXNL4A, 231 more genes
    nsv4676359copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,620,343-74,065,460 , GRCh38.p12 chr18: 68,953,106-76,353,505 TSHZ1, SMIM21, 70 more genes
    nsv4676287copy number variation1nstd102humanPathogenic GRCh37 chr18: 70,212,733-78,014,123 , GRCh38.p12 chr18: 72,545,498-80,256,240 ZNF236-DT, LOC105372221, 95 more genes
    nsv4676267copy number variation1nstd102humanPathogenic GRCh37 chr18: 70,383,594-78,014,123 , GRCh38.p12 chr18: 72,716,359-80,256,240 RN7SL551P, RN7SL401P, 93 more genes
    nsv4676250copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,994,711-74,293,556 , GRCh38.p12 chr18: 64,327,476-76,581,599 RNA5SP460, LINC01898, 104 more genes
    nsv4676246copy number variation1nstd102humanPathogenic GRCh37 chr18: 67,551,299-78,014,123 , GRCh38.p12 chr18: 69,884,063-80,256,240 ZNF407, ADNP2, 120 more genes
    nsv4676217copy number variation1nstd102humanPathogenic GRCh37 chr18: 60,098,018-78,014,123 , GRCh38.p12 chr18: 62,430,785-80,256,240 HNRNPA1P11, ZNF236, 184 more genes
    nsv4676158copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,458,425-78,014,123 , GRCh38.p12 chr18: 57,791,193-80,256,240 LOC105372140, LOC105372143, 253 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 MIR548AV, GTSCR1, 310 more genes
    nsv4625614copy number variation1nstd183human GRCh37 chr18: 71,814,375-71,818,190 , GRCh38.p12 chr18: 74,147,140-74,150,955 FBXO15, TIMM21
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