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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5905850copy number variation1nstd209human GRCh38 chr4: 184,811,363-184,820,267 , GRCh37.p13 chr4: 185,732,517-185,741,421 ACSL1
    nsv5838810copy number variation1nstd209human GRCh38 chr4: 184,811,370-184,820,404 , GRCh37.p13 chr4: 185,732,524-185,741,558 ACSL1
    nsv5838492copy number variation2nstd209human GRCh38 chr4: 184,818,705-184,819,804 , GRCh37.p13 chr4: 185,739,859-185,740,958 ACSL1
    nsv5838206copy number variation1nstd209human GRCh38 chr4: 184,788,588-184,789,987 , GRCh37.p13 chr4: 185,709,742-185,711,141 ACSL1
    nsv5692259mobile element insertion1nstd211human GRCh38 chr4: 184,825,099-184,825,099 , GRCh37.p13 chr4: 185,746,253-185,746,253 LOC105377587, ACSL1
    nsv5639119insertion1nstd207human GRCh38 chr4: 184,826,087-184,826,087 , GRCh37.p13 chr4: 185,747,241-185,747,241 ACSL1, LOC105377587
    nsv5543299insertion1nstd206human GRCh38 chr4: 184,826,152-184,826,155 , GRCh37.p13 chr4: 185,747,306-185,747,309 ACSL1, LOC105377587
    nsv5471699copy number variation1nstd206human GRCh38 chr4: 184,787,735-184,847,892 , GRCh37.p13 chr4: 185,708,889-185,769,046 MIR3945HG, ACSL1, 2 more genes
    nsv5455737copy number variation1nstd206human GRCh38 chr4: 184,811,343-184,820,315 , GRCh37.p13 chr4: 185,732,497-185,741,469 ACSL1
    nsv5454803copy number variation1nstd206human GRCh38 chr4: 184,212,885-185,009,149 , GRCh37.p13 chr4: 185,134,038-185,930,303 , RPL6P16, 22 more genes
    nsv5394618mobile element insertion1nstd206human GRCh38 chr4: 184,825,099-184,825,150 , GRCh37.p13 chr4: 185,746,253-185,746,304 ACSL1, LOC105377587
    nsv5377805translocation1nstd200human GRCh38 chr4: 184,775,673-184,775,673 , GRCh38 chr4: 184,776,526-184,776,526 , GRCh37.p13 chr4: 185,696,827-185,696,827 , GRCh37.p13 chr4: 185,697,680-185,697,680 ACSL1
    nsv5377803translocation1nstd200human GRCh38 chr4: 184,777,034-184,777,034 , GRCh38 chr4: 184,775,663-184,775,663 , GRCh37.p13 chr4: 185,696,817-185,696,817 , GRCh37.p13 chr4: 185,698,188-185,698,188 ACSL1
    nsv5367871translocation1nstd200human GRCh38 chr4: 187,241,301-187,241,301 , GRCh38 chr4: 184,811,409-184,811,409 , GRCh37.p13 chr4: 188,162,455-188,162,455 , GRCh37.p13 chr4: 185,732,563-185,732,563 LOC107986335, ACSL1
    nsv5345565translocation1nstd200human GRCh37 chr4: 185,696,827-185,696,827 , GRCh37 chr4: 185,697,680-185,697,680 , GRCh38.p12 chr4: 184,775,673-184,775,673 , GRCh38.p12 chr4: 184,776,526-184,776,526 ACSL1
    nsv5325087translocation1nstd204human GRCh38.p13 chr4: 184,776,526-184,776,526 , GRCh38.p13 chr4: 184,775,673-184,775,673 , GRCh37.p13 chr4: 185,696,827-185,696,827 , GRCh37.p13 chr4: 185,697,680-185,697,680 ACSL1
    nsv5324481translocation1nstd204human GRCh38.p13 chr4: 184,775,663-184,775,663 , GRCh38.p13 chr4: 184,777,034-184,777,034 , GRCh37.p13 chr4: 185,696,817-185,696,817 , GRCh37.p13 chr4: 185,698,188-185,698,188 ACSL1
    nsv5319226copy number variation1nstd204human GRCh38.p13 chr4: 184,811,344-184,812,405 , GRCh37.p13 chr4: 185,732,498-185,733,559 ACSL1
    nsv5239634copy number variation1nstd204human GRCh38.p13 chr4: 184,779,990-184,782,621 , GRCh37.p13 chr4: 185,701,144-185,703,775 ACSL1
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