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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7045397inversion1nstd229human GRCh38 chr6: 2,670,624-2,679,059 , GRCh37.p13 chr6: 2,670,858-2,679,293 MYLK4
    nsv7044205inversion1nstd229human GRCh38 chr6: 2,472,898-4,774,625 , GRCh37.p13 chr6: 2,473,132-4,774,859 TOMM5P1, PXDC1, 56 more genes
    nsv7042784inversion1nstd229human GRCh38 chr6: 2,599,103-2,898,736 , GRCh37.p13 chr6: 2,599,337-2,898,970 SERPINB1, SERPINB9P1, 7 more genes
    nsv6797975copy number variation1nstd229human GRCh38 chr6: 2,670,998-2,676,603 , GRCh37.p13 chr6: 2,671,232-2,676,837 MYLK4
    nsv6795135copy number variation1nstd229human GRCh38 chr6: 2,760,601-2,766,500 , GRCh37.p13 chr6: 2,760,835-2,766,734 MYLK4, WRNIP1
    nsv6787415copy number variation1nstd229human GRCh38 chr6: 2,702,847-2,702,900 , GRCh37.p13 chr6: 2,703,081-2,703,134 MYLK4
    nsv6785969copy number variation1nstd229human GRCh38 chr6: 2,699,998-2,707,845 , GRCh37.p13 chr6: 2,700,232-2,708,079 MYLK4
    nsv6785298copy number variation1nstd229human GRCh38 chr6: 2,759,301-4,105,800 , GRCh37.p13 chr6: 2,759,535-4,106,034 LOC107986557, SERPINB9-AS1, 39 more genes
    nsv6784602copy number variation1nstd229human GRCh38 chr6: 2,715,618-2,721,077 , GRCh37.p13 chr6: 2,715,852-2,721,311 MYLK4
    nsv6784114copy number variation1nstd229human GRCh38 chr6: 2,658,578-2,666,532 , GRCh37.p13 chr6: 2,658,812-2,666,766 MYLK4
    nsv6782658copy number variation1nstd229human GRCh38 chr6: 2,671,426-2,672,077 , GRCh37.p13 chr6: 2,671,660-2,672,311 MYLK4
    nsv6780018copy number variation1nstd229human GRCh38 chr6: 2,664,839-2,669,488 , GRCh37.p13 chr6: 2,665,073-2,669,722 MYLK4
    nsv6779811copy number variation1nstd229human GRCh38 chr6: 2,705,910-2,717,844 , GRCh37.p13 chr6: 2,706,144-2,718,078 MYLK4
    nsv6636569copy number variation1nstd102humanUncertain significance GRCh37 chr6: 2,162,500-2,864,248 , GRCh38.p12 chr6: 2,162,266-2,864,014 GMDS-DT, SERPINB9P1, 9 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
    nsv6631210copy number variation1nstd224human GRCh37 chr6: 1,633,682-2,893,647 , GRCh38.p12 chr6: 1,633,447-2,893,413 SERPINB1, SERPINB9P1, 12 more genes
    nsv6408070copy number variation1nstd223human GRCh38 chr6: 2,670,997-2,676,602 , GRCh37.p13 chr6: 2,671,231-2,676,836 MYLK4
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