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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7099026copy number variation1nstd102humanLikely benign GRCh37 chr2: 215,051,057-216,714,998 , GRCh38.p12 chr2: 214,186,333-215,850,275 LOC102724849, FN1-DT, 16 more genes
    nsv7057601inversion1nstd229human GRCh38 chr2: 215,635,748-215,640,691 , GRCh37.p13 chr2: 216,500,471-216,505,414 LINC00607, LOC102724861
    nsv7055266inversion1nstd229human GRCh38 chr2: 215,640,549-215,644,267 , GRCh37.p13 chr2: 216,505,272-216,508,990 LINC00607, LOC102724861
    nsv7054998inversion1nstd229human GRCh38 chr2: 213,756,606-215,928,356 , GRCh37.p13 chr2: 214,621,330-216,793,079 ABCA12, LINC00607, 19 more genes
    nsv7050394inversion1nstd229human GRCh38 chr2: 215,728,188-215,728,246 , GRCh37.p13 chr2: 216,592,911-216,592,969 LINC00607
    nsv7049220inversion1nstd229human GRCh38 chr2: 215,609,701-215,620,139 , GRCh37.p13 chr2: 216,474,424-216,484,862 LOC102724861, LINC00607
    nsv7047812inversion1nstd229human GRCh38 chr2: 215,654,176-215,654,286 , GRCh37.p13 chr2: 216,518,899-216,519,009 LOC102724861, LINC00607
    nsv7040681inversion1nstd229human GRCh38 chr2: 213,492,281-215,915,236 , GRCh37.p13 chr2: 214,357,005-216,779,959 LINC00607, LINC01614, 19 more genes
    nsv7039833inversion1nstd229human GRCh38 chr2: 215,609,774-215,614,425 , GRCh37.p13 chr2: 216,474,497-216,479,148 LOC102724861, LINC00607
    nsv6697895copy number variation1nstd229human GRCh38 chr2: 215,647,457-215,756,312 , GRCh37.p13 chr2: 216,512,180-216,621,035 LOC102724861, LINC01614, 1 more genes
    nsv6697459copy number variation1nstd229human GRCh38 chr2: 215,609,461-215,610,144 , GRCh37.p13 chr2: 216,474,184-216,474,867 LOC102724861, LINC00607
    nsv6697381copy number variation1nstd229human GRCh38 chr2: 215,609,322-215,610,162 , GRCh37.p13 chr2: 216,474,045-216,474,885 LOC102724861, LINC00607
    nsv6697300copy number variation1nstd229human GRCh38 chr2: 215,825,161-215,830,104 , GRCh37.p13 chr2: 216,689,884-216,694,827 LINC00607
    nsv6697023copy number variation1nstd229human GRCh38 chr2: 215,831,375-215,831,680 , GRCh37.p13 chr2: 216,696,098-216,696,403 LINC00607
    nsv6696331copy number variation1nstd229human GRCh38 chr2: 215,643,672-215,675,462 , GRCh37.p13 chr2: 216,508,395-216,540,185 LOC102724861, LINC00607
    nsv6696180copy number variation1nstd229human GRCh38 chr2: 215,699,282-215,699,340 , GRCh37.p13 chr2: 216,564,005-216,564,063 LINC00607
    nsv6695795copy number variation1nstd229human GRCh38 chr2: 215,682,903-215,682,962 , GRCh37.p13 chr2: 216,547,626-216,547,685 LINC00607, LOC102724861
    nsv6695064copy number variation1nstd229human GRCh38 chr2: 215,783,848-215,784,969 , GRCh37.p13 chr2: 216,648,571-216,649,692 LINC00607
    nsv6693693copy number variation1nstd229human GRCh38 chr2: 215,789,801-215,793,500 , GRCh37.p13 chr2: 216,654,524-216,658,223 LINC00607
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