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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7051552inversion1nstd229human GRCh38 chr6: 11,086,774-14,472,374 , GRCh37.p13 chr6: 11,087,007-14,472,605 LOC105374933, ADTRP, 53 more genes
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6798011copy number variation1nstd229human GRCh38 chr6: 11,712,054-11,723,864 , GRCh37.p13 chr6: 11,712,287-11,724,097 ADTRP
    nsv6797529copy number variation1nstd229human GRCh38 chr6: 11,776,301-11,781,000 , GRCh37.p13 chr6: 11,776,534-11,781,233 ADTRP
    nsv6791051copy number variation1nstd229human GRCh38 chr6: 11,775,127-11,775,199 , GRCh37.p13 chr6: 11,775,360-11,775,432 ADTRP
    nsv6788112copy number variation1nstd229human GRCh38 chr6: 11,773,875-11,776,066 , GRCh37.p13 chr6: 11,774,108-11,776,299 ADTRP
    nsv6787714copy number variation1nstd229human GRCh38 chr6: 11,675,101-11,729,500 , GRCh37.p13 chr6: 11,675,334-11,729,733 ADTRP, LOC340184
    nsv6787023copy number variation1nstd229human GRCh38 chr6: 11,771,090-11,771,115 , GRCh37.p13 chr6: 11,771,323-11,771,348 ADTRP
    nsv6786901copy number variation1nstd229human GRCh38 chr6: 11,726,290-11,732,050 , GRCh37.p13 chr6: 11,726,523-11,732,283 ADTRP
    nsv6785724copy number variation1nstd229human GRCh38 chr6: 11,735,713-11,735,899 , GRCh37.p13 chr6: 11,735,946-11,736,132 ADTRP
    nsv6783089copy number variation1nstd229human GRCh38 chr6: 11,675,030-11,729,571 , GRCh37.p13 chr6: 11,675,263-11,729,804 LOC340184, ADTRP
    nsv6782055copy number variation1nstd229human GRCh38 chr6: 11,723,143-11,725,729 , GRCh37.p13 chr6: 11,723,376-11,725,962 ADTRP
    nsv6409723copy number variation1nstd223human GRCh38 chr6: 7,366,072-12,459,745 , GRCh37.p13 chr6: 7,366,305-12,459,977 EEF1E1, RPS26P29, 82 more genes
    nsv6408134copy number variation1nstd223human GRCh38 chr6: 11,760,201-11,761,300 , GRCh37.p13 chr6: 11,760,434-11,761,533 ADTRP
    nsv6404257copy number variation1nstd223human GRCh38 chr6: 11,756,710-11,757,089 , GRCh37.p13 chr6: 11,756,943-11,757,322 ADTRP
    nsv6315320copy number variation1nstd102humanUncertain significance GRCh38 chr6: 11,481,309-12,522,879 , GRCh37.p13 chr6: 11,481,542-12,523,111 ADTRP, HIVEP1, 15 more genes
    nsv6135707copy number variation1nstd213human GRCh37 chr6: 11,010,000-11,730,001 , GRCh38.p12 chr6: 11,009,767-11,729,768 SMIM13, THAP12P5, 13 more genes
    nsv6135469copy number variation1nstd213human GRCh37 chr6: 11,730,000-19,840,001 , GRCh38.p12 chr6: 11,729,767-19,839,770 EDN1, GMPR, 115 more genes
    nsv5466688copy number variation1nstd206human GRCh38 chr6: 11,775,127-11,775,199 , GRCh37.p13 chr6: 11,775,360-11,775,432 ADTRP
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