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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 more genes
    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
    nsv5662670insertion1nstd207human GRCh38 chr18: 3,421,221-3,421,221 , GRCh37.p13 chr18: 3,421,219-3,421,219 TGIF1
    nsv5533353copy number variation1nstd206human GRCh38 chr18: 3,422,666-3,422,763 , GRCh37.p13 chr18: 3,422,664-3,422,761 TGIF1
    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
    nsv5530357copy number variation1nstd206human GRCh38 chr18: 3,452,018-3,453,412 , GRCh37.p13 chr18: 3,452,016-3,453,410 TGIF1
    nsv5529974copy number variation1nstd206human GRCh38 chr18: 3,442,010-3,442,130 , GRCh37.p13 chr18: 3,442,008-3,442,128 TGIF1
    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
    nsv5290248copy number variation1nstd204human GRCh38.p13 chr18: 3,422,381-3,443,689 , GRCh37.p13 chr18: 3,422,379-3,443,687 TGIF1
    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
    nsv5154938mobile element insertion1nstd203human GRCh38 chr18: 3,434,536-3,434,552 , GRCh37.p13 chr18: 3,434,534-3,434,550 TGIF1
    nsv5149721mobile element insertion1nstd203human GRCh38 chr18: 3,448,035-3,448,050 , GRCh37.p13 chr18: 3,448,033-3,448,048 TGIF1
    nsv5017338copy number variation1nstd200human GRCh38 chr18: 3,426,557-3,426,722 , GRCh37.p13 chr18: 3,426,555-3,426,720 TGIF1
    nsv5017337copy number variation1nstd200human GRCh38 chr18: 3,421,948-3,423,406 , GRCh37.p13 chr18: 3,421,946-3,423,404 TGIF1
    nsv5017336copy number variation1nstd200human GRCh38 chr18: 3,421,706-3,422,928 , GRCh37.p13 chr18: 3,421,704-3,422,926 TGIF1
    nsv5017335copy number variation1nstd200human GRCh38 chr18: 3,416,760-3,421,989 , GRCh37.p13 chr18: 3,416,758-3,421,987 BOD1P1, TGIF1
    nsv5014207copy number variation1nstd200human GRCh38 chr18: 3,382,040-4,031,001 , GRCh37.p13 chr18: 3,382,038-4,031,001 , GAPDHP66, 16 more genes
    nsv4867727copy number variation1nstd200human GRCh37 chr18: 3,421,956-3,423,404 , GRCh38.p12 chr18: 3,421,958-3,423,406 TGIF1
    nsv4867726copy number variation1nstd200human GRCh37 chr18: 3,416,782-3,422,012 , GRCh38.p12 chr18: 3,416,784-3,422,014 TGIF1
    nsv4854496copy number variation1nstd200human GRCh37 chr18: 3,382,038-4,031,001 , GRCh38.p12 chr18: 3,382,040-4,031,001 , BOD1P1, 16 more genes
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