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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124744copy number variation1nstd186human GRCh37 chr18: 3,272,249-3,272,300 , GRCh38.p12 chr18: 3,272,251-3,272,302 MYL12B
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 more genes
    nsv5938153copy number variation1nstd209human GRCh38 chr18: 3,272,251-3,272,302 , GRCh37.p13 chr18: 3,272,249-3,272,300 MYL12B
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5646376insertion1nstd207human GRCh38 chr18: 3,272,251-3,272,251 , GRCh37.p13 chr18: 3,272,249-3,272,249 MYL12B
    nsv5531364copy number variation1nstd206human GRCh38 chr18: 3,206,000-3,412,000 , GRCh37.p13 chr18: 3,205,998-3,411,998 MYOM1, TGIF1, 8 more genes
    nsv5526125copy number variation1nstd206human GRCh38 chr18: 3,272,251-3,272,302 , GRCh37.p13 chr18: 3,272,249-3,272,300 MYL12B
    nsv5518861copy number variation1nstd206human GRCh38 chr18: 3,275,061-3,275,820 , GRCh37.p13 chr18: 3,275,059-3,275,818 MYL12B
    nsv5359058translocation1nstd200human GRCh38 chr18: 3,275,061-3,275,061 , GRCh38 chr18: 3,275,820-3,275,820 , GRCh37.p13 chr18: 3,275,059-3,275,059 , GRCh37.p13 chr18: 3,275,818-3,275,818 MYL12B
    nsv5330908translocation1nstd200human GRCh37 chr18: 3,275,059-3,275,059 , GRCh37 chr18: 3,275,818-3,275,818 , GRCh38.p12 chr18: 3,275,061-3,275,061 , GRCh38.p12 chr18: 3,275,820-3,275,820 MYL12B
    nsv5321644copy number variation1nstd204human GRCh38.p13 chr18: 2,770,369-3,867,276 , GRCh37.p13 chr18: 2,770,367-3,867,276 , MYL12B, 25 more genes
    nsv5286052copy number variation1nstd204human GRCh38.p13 chr18: 2,770,801-3,600,700 , GRCh37.p13 chr18: 2,770,799-3,600,698 LPIN2, LOC100419892, 22 more genes
    nsv5145167mobile element insertion1nstd203human GRCh38 chr18: 3,278,046-3,278,060 , GRCh37.p13 chr18: 3,278,044-3,278,058 MYL12B
    nsv5017326copy number variation1nstd200human GRCh38 chr18: 3,268,161-3,268,961 , GRCh37.p13 chr18: 3,268,159-3,268,959 MYL12B
    nsv5014202copy number variation1nstd200human GRCh38 chr18: 3,096,086-3,385,261 , GRCh37.p13 chr18: 3,096,084-3,385,259 MYL12A, LOC101927044, 5 more genes
    nsv4867719copy number variation1nstd200human GRCh37 chr18: 3,268,159-3,268,959 , GRCh38.p12 chr18: 3,268,161-3,268,961 MYL12B
    nsv4854494copy number variation1nstd200human GRCh37 chr18: 3,096,084-3,385,259 , GRCh38.p12 chr18: 3,096,086-3,385,261 MYOM1, LINC01895, 5 more genes
    nsv4854492copy number variation1nstd200human GRCh37 chr18: 2,770,703-3,867,127 , GRCh38.p12 chr18: 2,770,705-3,867,127 , SMCHD1, 25 more genes
    nsv4761861insertion1nstd199human GRCh37 chr18: 3,272,250-3,272,250 , GRCh38.p12 chr18: 3,272,252-3,272,252 MYL12B
    nsv4729860copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-3,415,478 , GRCh38.p12 chr18: 136,226-3,415,480 AIDAP3, LOC105371963, 56 more genes
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