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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962373insertion1nstd209human GRCh38 chr6: 147,956-147,956 , GRCh37.p13 chr6: 147,956-147,956
    nsv5902877copy number variation1nstd209human GRCh38 chr6: 147,657-147,707 , GRCh37.p13 chr6: 147,657-147,707
    nsv5902169copy number variation1nstd209human GRCh38 chr6: 148,413-148,470 , GRCh37.p13 chr6: 148,413-148,470
    nsv5899646copy number variation1nstd209human GRCh38 chr6: 148,624-148,866 , GRCh37.p13 chr6: 148,624-148,866
    nsv5667789inversion1nstd207human GRCh38 chr6: 10,002-144,018 , GRCh37.p13 chr6: 60,001-144,018 , OR4F1P, 4 more genes
    nsv5635489insertion1nstd207human GRCh38 chr6: 147,907-147,907 , GRCh37.p13 chr6: 147,907-147,907
    nsv5580389copy number variation1nstd207human GRCh38 chr6: 147,657-147,707 , GRCh37.p13 chr6: 147,657-147,707
    nsv5549956insertion1nstd206human GRCh38 chr6: 147,936-147,936 , GRCh37.p13 chr6: 147,936-147,936
    nsv5460400copy number variation1nstd206human GRCh38 chr6: 80,000-1,240,000 , GRCh37.p13 chr6: 80,000-1,240,235 , CICP18, 18 more genes
    nsv5240169copy number variation1nstd204human GRCh38.p13 chr6: 143,301-144,200 , GRCh37.p13 chr6: 143,301-144,200 , CICP18
    nsv5237997copy number variation1nstd204human GRCh38.p13 chr6: 143,401-146,600 , GRCh37.p13 chr6: 143,401-146,600 , CICP18
    nsv5237603copy number variation1nstd204human GRCh38.p13 chr6: 134,301-141,500 , GRCh37.p13 chr6: 134,301-141,500 , CICP18, 1 more genes
    nsv5234875copy number variation1nstd204human GRCh38.p13 chr6: 144,901-146,100 , GRCh37.p13 chr6: 144,901-146,100 , CICP18
    nsv5233066copy number variation1nstd204human GRCh38.p13 chr6: 142,101-147,400 , GRCh37.p13 chr6: 142,101-147,400 , CICP18
    nsv5231048copy number variation1nstd204human GRCh38.p13 chr6: 143,401-147,900 , GRCh37.p13 chr6: 143,401-147,900 , CICP18
    nsv5230949copy number variation1nstd204human GRCh38.p13 chr6: 136,701-139,000 , GRCh37.p13 chr6: 136,701-139,000 , SEPTIN14P6
    nsv5230164copy number variation1nstd204human GRCh38.p13 chr6: 123,801-147,800 , GRCh37.p13 chr6: 123,801-147,800 , SEPTIN14P6, 1 more genes
    nsv5228709copy number variation1nstd204human GRCh38.p13 chr6: 131,501-147,800 , GRCh37.p13 chr6: 131,501-147,800 , CICP18, 1 more genes
    nsv5227906copy number variation1nstd204human GRCh38.p13 chr6: 134,301-147,800 , GRCh37.p13 chr6: 134,301-147,800 , SEPTIN14P6, 1 more genes
    nsv5225657copy number variation1nstd204human GRCh38.p13 chr6: 126,501-147,800 , GRCh37.p13 chr6: 126,501-147,800 , SEPTIN14P6, 1 more genes
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