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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
    nsv5934134copy number variation1nstd209human GRCh38 chr18: 70,650,159-70,651,035 , GRCh37.p13 chr18: 68,317,395-68,318,271 GTSCR1
    nsv5715900mobile element insertion2nstd211human GRCh38 chr18: 70,650,380-70,650,380 , GRCh37.p13 chr18: 68,317,616-68,317,616 GTSCR1
    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
    nsv5170707mobile element insertion1nstd203human GRCh38 chr18: 70,650,351-70,650,380 , GRCh37.p13 chr18: 68,317,587-68,317,616 GTSCR1
    nsv4854794copy number variation1nstd200human GRCh37 chr18: 68,316,822-68,944,366 , GRCh38.p12 chr18: 70,649,586-71,277,130 , GTSCR1, 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
    nsv4729838copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 65,736,299-69,297,115 , GRCh38.p12 chr18: 68,069,062-71,629,879 MTL3P, SOCS6, 31 more genes
    nsv4729787copy number variation1nstd102humanUncertain significance GRCh37 chr18: 66,697,605-69,608,331 , GRCh38.p12 chr18: 69,030,368-71,941,095 GTSCR1, LIVAR, 28 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
    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
    nsv4676216copy number variation1nstd102humanUncertain significance GRCh37 chr18: 64,809,285-68,568,490 , GRCh38.p12 chr18: 67,142,048-70,901,254 GTSCR1, RNU6-39P, 34 more genes
    nsv4676160copy number variation1nstd102humanUncertain significance GRCh37 chr18: 68,238,848-69,881,714 , GRCh38.p12 chr18: 70,571,612-72,214,479 LINC01899, LOC100132647, 11 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
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