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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137073copy number variation1nstd102humanPathogenic GRCh37 chr6: 491,126-1,624,775 , GRCh38.p12 chr6: 491,126-1,624,540 RN7SL352P, LOC107986555, 18 more genes
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7097816copy number variation1nstd102humanPathogenic GRCh37 chr6: 1,609,367-1,610,939 , GRCh38.p12 chr6: 1,609,132-1,610,704 FOXC1
    nsv7097052copy number variation1nstd102humanPathogenic GRCh37 chr6: 1,610,666-1,612,017 , GRCh38.p12 chr6: 1,610,431-1,611,782 FOXC1
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7093107copy number variation1nstd102humanPathogenic GRCh37 chr6: 1,611,469-1,611,470 , GRCh38 chr6: 1,611,234-1,611,235 FOXC1
    nsv7052975inversion1nstd229human GRCh38 chr6: 1,604,649-1,608,195 , GRCh37.p13 chr6: 1,604,884-1,608,430 FOXCUT, FOXC1
    nsv6791546copy number variation1nstd229human GRCh38 chr6: 1,355,405-2,241,325 , GRCh37.p13 chr6: 1,355,640-2,241,559 FOXF2-DT, LOC105374883, 11 more genes
    nsv6789395copy number variation1nstd229human GRCh38 chr6: 1,598,488-1,608,195 , GRCh37.p13 chr6: 1,598,723-1,608,430 FOXCUT, FOXC1
    nsv6783497copy number variation1nstd229human GRCh38 chr6: 1,607,190-1,609,831 , GRCh37.p13 chr6: 1,607,425-1,610,066 FOXCUT, FOXC1
    nsv6781953copy number variation1nstd229human GRCh38 chr6: 1,230,370-1,734,614 , GRCh37.p13 chr6: 1,230,605-1,734,848 LINC01394, LOC102723944, 13 more genes
    nsv6780017copy number variation1nstd229human GRCh38 chr6: 1,572,001-1,854,500 , GRCh37.p13 chr6: 1,572,236-1,854,734 GMDS, FOXCUT, 3 more genes
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6630921copy number variation1nstd224human GRCh37 chr6: 1,149,856-1,613,686 , GRCh38.p12 chr6: 1,149,621-1,613,451 FOXF2, FOXCUT, 11 more genes
    nsv6408963copy number variation1nstd223human GRCh38 chr6: 1,232,014-1,776,081 , GRCh37.p13 chr6: 1,232,249-1,776,315 FOXC1, LOC102723944, 13 more genes
    nsv6398696copy number variation1nstd223human GRCh38 chr6: 1,205,201-1,848,200 , GRCh37.p13 chr6: 1,205,436-1,848,434 LOC105374879, FOXC1, 13 more genes
    nsv6398501copy number variation1nstd223human GRCh38 chr6: 1,466,398-1,647,557 , GRCh37.p13 chr6: 1,466,633-1,647,791 FOXC1, GMDS, 6 more genes
    nsv6314746copy number variation1nstd102humanPathogenic GRCh37 chr6: 375,263-3,655,142 , GRCh38.p12 chr6: 375,263-3,654,908 RN7SL352P, SERPINB8P1, 55 more genes
    nsv6313856copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,527,437-1,764,940 , GRCh38.p12 chr6: 1,527,202-1,764,706 FOXC1, LOC102723944, 4 more genes
    nsv6313679copy number variation1nstd102humanPathogenic GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385 SERPINB9P1, LOC101927691, 59 more genes
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