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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5968178insertion1nstd209human GRCh38 chr18: 46,494,846-46,494,846 , GRCh37.p13 chr18: 44,074,809-44,074,809 LOXHD1
    nsv5708111mobile element insertion2nstd211human GRCh38 chr18: 46,596,165-46,596,165 , GRCh37.p13 chr18: 44,176,128-44,176,128 LOXHD1
    nsv5695807mobile element insertion1nstd211human GRCh38 chr18: 46,516,255-46,516,255 , GRCh37.p13 chr18: 44,096,218-44,096,218 LOXHD1
    nsv5674238insertion1nstd102humanPathogenic GRCh37 chr18: 44,125,328-44,125,328 , GRCh38 chr18: 46,545,365-46,545,365 LOXHD1
    nsv5673059copy number variation1nstd102humanPathogenic GRCh37 chr18: 44,087,491-44,089,788 , GRCh38.p12 chr18: 46,507,528-46,509,825 LOXHD1
    nsv5654579insertion1nstd207human GRCh38 chr18: 46,556,766-46,556,766 , GRCh37.p13 chr18: 44,136,729-44,136,729 LOXHD1
    nsv5653055insertion1nstd207human GRCh38 chr18: 46,546,293-46,546,293 , GRCh37.p13 chr18: 44,126,256-44,126,256 LOXHD1
    nsv5552844insertion1nstd206human GRCh38 chr18: 46,556,764-46,556,766 , GRCh37.p13 chr18: 44,136,727-44,136,729 LOXHD1
    nsv5548170insertion1nstd206human GRCh38 chr18: 46,556,812-46,556,817 , GRCh37.p13 chr18: 44,136,775-44,136,780 LOXHD1
    nsv5546893insertion1nstd206human GRCh38 chr18: 46,608,055-46,608,057 , GRCh37.p13 chr18: 44,188,018-44,188,020 LOXHD1
    nsv5536137insertion1nstd206human GRCh38 chr18: 46,590,179-46,590,179 , GRCh37.p13 chr18: 44,170,142-44,170,142 LOXHD1
    nsv5530873copy number variation1nstd206human GRCh38 chr18: 46,487,102-46,487,169 , GRCh37.p13 chr18: 44,067,065-44,067,132 LOXHD1
    nsv5530435copy number variation1nstd206human GRCh38 chr18: 46,559,409-46,561,512 , GRCh37.p13 chr18: 44,139,372-44,141,475 LOXHD1
    nsv5526017copy number variation1nstd206human GRCh38 chr18: 46,642,903-46,683,958 , GRCh37.p13 chr18: 44,222,866-44,263,921 LOXHD1, LOC105372096, 1 more genes
    nsv5519300copy number variation1nstd206human GRCh38 chr18: 46,500,226-46,505,369 , GRCh37.p13 chr18: 44,080,189-44,085,332 LOXHD1
    nsv5515284copy number variation1nstd206human GRCh38 chr18: 46,505,621-46,505,678 , GRCh37.p13 chr18: 44,085,584-44,085,641 LOXHD1
    nsv5415643mobile element insertion1nstd206human GRCh38 chr18: 46,596,165-46,596,216 , GRCh37.p13 chr18: 44,176,128-44,176,179 LOXHD1
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
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