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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
    nsv5946456copy number variation1nstd209human GRCh38 chr18: 58,730,759-58,731,008 , GRCh37.p13 chr18: 56,397,991-56,398,240 MALT1
    nsv5942676copy number variation1nstd209human GRCh38 chr18: 58,704,724-58,705,024 , GRCh37.p13 chr18: 56,371,956-56,372,256 MALT1
    nsv5730757mobile element insertion1nstd211human GRCh38 chr18: 58,677,983-58,677,983 , GRCh37.p13 chr18: 56,345,215-56,345,215 LOC105372146, MALT1
    nsv5713506mobile element insertion1nstd211human GRCh38 chr18: 58,727,642-58,727,642 , GRCh37.p13 chr18: 56,394,874-56,394,874 MALT1
    nsv5519711copy number variation1nstd206human GRCh38 chr18: 58,744,980-58,745,039 , GRCh37.p13 chr18: 56,412,212-56,412,271 MALT1
    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
    nsv5381190copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,225,777-56,940,458 , GRCh38.p12 chr18: 57,558,545-59,273,226 TRG-TCC6-1, RAX, 32 more genes
    nsv5199141mobile element insertion1nstd203human GRCh38 chr18: 58,688,244-58,688,259 , GRCh37.p13 chr18: 56,355,476-56,355,491 LOC105372146, MALT1
    nsv5150986mobile element insertion1nstd203human GRCh38 chr18: 58,740,452-58,740,466 , GRCh37.p13 chr18: 56,407,684-56,407,698 MALT1
    nsv5024251copy number variation1nstd200human GRCh38 chr18: 58,715,884-58,826,758 , GRCh37.p13 chr18: 56,383,116-56,493,990 RNU6-219P, LINC01926, 1 more genes
    nsv5018300copy number variation1nstd200human GRCh38 chr18: 58,748,606-58,750,231 , GRCh37.p13 chr18: 56,415,838-56,417,463 MALT1
    nsv5018299copy number variation1nstd200human GRCh38 chr18: 58,710,943-58,711,026 , GRCh37.p13 chr18: 56,378,175-56,378,258 MALT1
    nsv5018298copy number variation1nstd200human GRCh38 chr18: 58,707,291-58,708,235 , GRCh37.p13 chr18: 56,374,523-56,375,467 MALT1
    nsv5018297copy number variation1nstd200human GRCh38 chr18: 58,689,501-58,693,011 , GRCh37.p13 chr18: 56,356,733-56,360,243 MALT1, MRPL37P1, 1 more genes
    nsv4859780copy number variation1nstd200human GRCh37 chr18: 56,374,523-56,375,467 , GRCh38.p12 chr18: 58,707,291-58,708,235 MALT1
    nsv4854726copy number variation1nstd200human GRCh37 chr18: 56,383,116-56,493,990 , GRCh38.p12 chr18: 58,715,884-58,826,758 RNU6-219P, LINC01926, 1 more genes
    nsv4682744copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr18: 56,338,856-56,415,094 , GRCh38.p12 chr18: 58,671,624-58,747,862 LOC105372146, MALT1, 2 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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