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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7137137copy number variation1nstd102humanPathogenic GRCh37 chr18: 71,740,696-78,005,231 , GRCh38.p12 chr18: 74,073,461-80,247,348 LOC339298, LOC105372201, 84 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7012114copy number variation1nstd229human GRCh38 chr18: 76,111,273-76,122,449 , GRCh37.p13 chr18: 73,823,228-73,834,404 LOC339298
    nsv7011737copy number variation1nstd229human GRCh38 chr18: 76,139,874-76,139,999 , GRCh37.p13 chr18: 73,851,829-73,851,954 LOC339298
    nsv7006150copy number variation1nstd229human GRCh38 chr18: 76,144,583-76,269,560 , GRCh37.p13 chr18: 73,856,538-73,981,515 LOC105372210, LINC01893, 3 more genes
    nsv7006143copy number variation1nstd229human GRCh38 chr18: 76,068,701-76,270,200 , GRCh37.p13 chr18: 73,780,656-73,982,155 LOC105372210, LINC01893, 3 more genes
    nsv7005551copy number variation1nstd229human GRCh38 chr18: 76,120,879-76,121,012 , GRCh37.p13 chr18: 73,832,834-73,832,967 LOC339298
    nsv7000238copy number variation1nstd229human GRCh38 chr18: 76,110,470-76,204,580 , GRCh37.p13 chr18: 73,822,425-73,916,535 LOC339298, LOC105372206
    nsv6998445copy number variation1nstd229human GRCh38 chr18: 76,124,628-76,125,055 , GRCh37.p13 chr18: 73,836,583-73,837,010 LOC339298
    nsv6638045copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240 LOC105372211, LOC105372188, 128 more genes
    nsv6638004copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,520,071-78,014,123 , GRCh38.p12 chr18: 63,852,837-80,256,240 LOC107985151, CD226, 165 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
    nsv6637395copy number variation1nstd102humanUncertain significance GRCh37 chr18: 73,711,236-74,360,445 , GRCh38.p12 chr18: 75,999,281-76,648,488 LOC105372204, LOC339298, 12 more genes
    nsv6634444copy number variation1nstd102humanPathogenic GRCh37 chr18: 72,669,936-77,889,946 , GRCh38.p12 chr18: 74,957,980-80,132,063 LOC105372212, GALR1, 71 more genes
    nsv6529577copy number variation1nstd223human GRCh38 chr18: 76,132,620-76,133,299 , GRCh37.p13 chr18: 73,844,575-73,845,254 LOC339298
    nsv6315531copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,289,055-78,014,123 , GRCh38.p12 chr18: 63,621,821-80,256,240 RN7SL795P, ZNF407, 169 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315301copy number variation1nstd102humanPathogenic GRCh38 chr18: 61,490,305-80,247,612 , GRCh37.p13 chr18: 59,157,538-78,005,495 RN7SL705P, LOC105372166, 196 more genes
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