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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966029insertion1nstd209human GRCh38 chr2: 131,364,113-131,364,113 , GRCh37.p13 chr2: 132,121,686-132,121,686 RAB6D
    nsv5831567copy number variation2nstd209human GRCh38 chr2: 131,356,429-131,380,613 , GRCh37.p13 chr2: 132,114,002-132,138,186 MTND5P23, MTND3P18, 9 more genes
    nsv5831564copy number variation2nstd209human GRCh38 chr2: 131,352,886-131,362,013 , GRCh37.p13 chr2: 132,110,459-132,119,586 SSBP3P2, LOC100420006, 1 more genes
    nsv5665937inversion1nstd207human GRCh38 chr2: 130,138,213-131,531,319 , GRCh37.p13 chr2: 130,895,786-132,288,892 , GNAQP1, 84 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449752copy number variation1nstd206human GRCh38 chr2: 131,233,309-131,501,809 , GRCh37.p13 chr2: 131,990,882-132,259,177 SMPD4BP, MTND3P18, 31 more genes
    nsv5443477copy number variation1nstd206human GRCh38 chr2: 131,208,618-131,391,809 , GRCh37.p13 chr2: 131,966,191-132,149,382 , MTND2P18, 24 more genes
    nsv5437602copy number variation1nstd206human GRCh38 chr2: 131,208,309-131,740,809 , GRCh37.p13 chr2: 131,965,882-132,498,382 , LINC01120, 42 more genes
    nsv5434286copy number variation1nstd206human GRCh38 chr2: 131,208,118-131,540,100 , GRCh37.p13 chr2: 131,965,691-132,297,673 , MTND2P18, 35 more genes
    nsv5327037inversion1nstd204human GRCh37.p13 chr2: 130,942,902-132,247,079 , GRCh38.p13 chr2: 130,185,329-131,489,506 , PTPN18, 79 more genes
    nsv5075896mobile element insertion1nstd203human GRCh38 chr2: 131,361,695-131,361,704 , GRCh37.p13 chr2: 132,119,268-132,119,277 RAB6D
    nsv5037689inversion1nstd200human GRCh38 chr2: 130,226,386-131,459,405 , GRCh37.p13 chr2: 130,983,959-132,216,978 , MTND6P10, 73 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4926075copy number variation1nstd200human GRCh38 chr2: 130,830,344-131,824,388 , GRCh37.p13 chr2: 131,587,917-132,581,961 , LOC112268425, 50 more genes
    nsv4923974copy number variation1nstd200human GRCh38 chr2: 131,099,303-132,437,777 , GRCh37.p13 chr2: 131,856,876-133,195,350 , MTND4P21, 67 more genes
    nsv4889214inversion1nstd200human GRCh37 chr2: 130,983,959-132,216,978 , GRCh38.p12 chr2: 130,226,386-131,459,405 , KLF2P2, 73 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4770868copy number variation1nstd200human GRCh37 chr2: 131,587,942-132,581,943 , GRCh38.p12 chr2: 130,830,369-131,824,370 , ARHGEF4, 50 more genes
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