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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
    nsv5515984copy number variation1nstd206human GRCh38 chr18: 72,632,069-72,632,119 , GRCh37.p13 chr18: 70,299,304-70,299,354 CBLN2
    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
    nsv5375252translocation1nstd200human GRCh38 chr18: 72,636,429-72,636,429 , GRCh38 chr18: 68,763,639-68,763,639 , GRCh37.p13 chr18: 66,430,876-66,430,876 , GRCh37.p13 chr18: 70,303,664-70,303,664 CCDC102B, CBLN2
    nsv5375249translocation1nstd200human GRCh38 chr18: 67,838,448-67,838,448 , GRCh38 chr18: 72,558,414-72,558,414 , GRCh37.p13 chr18: 65,505,685-65,505,685 , GRCh37.p13 chr18: 70,225,649-70,225,649 CBLN2, DSEL-AS1
    nsv5375248translocation1nstd200human GRCh38 chr18: 67,838,372-67,838,372 , GRCh38 chr18: 72,557,488-72,557,488 , GRCh37.p13 chr18: 65,505,609-65,505,609 , GRCh37.p13 chr18: 70,224,723-70,224,723 CBLN2, DSEL-AS1
    nsv5359282translocation1nstd200human GRCh38 chr18: 72,630,607-72,630,607 , GRCh38 chr18: 72,630,541-72,630,541 , GRCh37.p13 chr18: 70,297,776-70,297,776 , GRCh37.p13 chr18: 70,297,842-70,297,842 CBLN2
    nsv5343282translocation1nstd200human GRCh37 chr18: 70,297,776-70,297,776 , GRCh37 chr18: 70,297,842-70,297,842 , GRCh38.p12 chr18: 72,630,541-72,630,541 , GRCh38.p12 chr18: 72,630,607-72,630,607 CBLN2
    nsv5339188translocation1nstd200human GRCh37 chr18: 70,259,273-70,259,273 , GRCh37 chr18: 70,259,327-70,259,327 , GRCh38.p12 chr18: 72,592,092-72,592,092 , GRCh38.p12 chr18: 72,592,038-72,592,038 CBLN2
    nsv5322756copy number variation1nstd204human GRCh38.p13 chr18: 72,617,597-72,665,628 , GRCh37.p13 chr18: 70,284,832-70,332,863 HNRNPA1P11, CBLN2
    nsv5286419copy number variation1nstd204human GRCh38.p13 chr18: 72,618,127-72,650,934 , GRCh37.p13 chr18: 70,285,362-70,318,169 HNRNPA1P11, CBLN2
    nsv5170373mobile element insertion1nstd203human GRCh38 chr18: 72,624,863-72,624,875 , GRCh37.p13 chr18: 70,292,098-70,292,110 CBLN2
    nsv5027081copy number variation1nstd200human GRCh38 chr18: 72,605,520-72,605,628 , GRCh37.p13 chr18: 70,272,755-70,272,863 CBLN2
    nsv5027080copy number variation1nstd200human GRCh38 chr18: 72,592,038-72,592,092 , GRCh37.p13 chr18: 70,259,273-70,259,327 CBLN2
    nsv5027079copy number variation1nstd200human GRCh38 chr18: 72,551,979-72,573,518 , GRCh37.p13 chr18: 70,219,214-70,240,753 CBLN2
    nsv5027078copy number variation1nstd200human GRCh38 chr18: 72,531,106-72,537,829 , GRCh37.p13 chr18: 70,198,341-70,205,064 CBLN2
    nsv5024392copy number variation1nstd200human GRCh38 chr18: 72,617,607-72,665,619 , GRCh37.p13 chr18: 70,284,842-70,332,854 CBLN2, HNRNPA1P11
    nsv4860202copy number variation1nstd200human GRCh37 chr18: 70,219,214-70,240,753 , GRCh38.p12 chr18: 72,551,979-72,573,518 CBLN2
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