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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894405copy number variation1nstd209human GRCh38 chr6: 37,639,111-37,639,167 , GRCh37.p13 chr6: 37,606,887-37,606,943 MDGA1
    nsv5630619insertion1nstd207human GRCh38 chr6: 37,664,842-37,664,842 , GRCh37.p13 chr6: 37,632,618-37,632,618 MDGA1
    nsv5627712insertion1nstd207human GRCh38 chr6: 37,698,244-37,698,244 , GRCh37.p13 chr6: 37,666,020-37,666,020 MDGA1
    nsv5626840insertion1nstd207human GRCh38 chr6: 37,644,069-37,644,069 , GRCh37.p13 chr6: 37,611,845-37,611,845 MDGA1
    nsv5572049copy number variation1nstd207human GRCh38 chr6: 37,644,050-37,644,146 , GRCh37.p13 chr6: 37,611,826-37,611,922 MDGA1
    nsv5462846copy number variation1nstd206human GRCh38 chr6: 37,644,089-37,644,147 , GRCh37.p13 chr6: 37,611,865-37,611,923 MDGA1
    nsv5461884copy number variation1nstd206human GRCh38 chr6: 37,670,372-37,670,711 , GRCh37.p13 chr6: 37,638,148-37,638,487 MDGA1
    nsv5378410translocation1nstd200human GRCh38 chr6: 37,675,766-37,675,766 , GRCh38 chr6: 37,677,627-37,677,627 , GRCh37.p13 chr6: 37,645,403-37,645,403 , GRCh37.p13 chr6: 37,643,542-37,643,542 MDGA1
    nsv5362863translocation1nstd200human GRCh38 chr6: 37,693,958-37,693,958 , GRCh38 chr6: 37,694,855-37,694,855 , GRCh37.p13 chr6: 37,662,631-37,662,631 , GRCh37.p13 chr6: 37,661,734-37,661,734 MDGA1
    nsv5339329translocation1nstd200human GRCh37 chr6: 37,643,542-37,643,542 , GRCh37 chr6: 37,645,403-37,645,403 , GRCh38.p12 chr6: 37,675,766-37,675,766 , GRCh38.p12 chr6: 37,677,627-37,677,627 MDGA1
    nsv5335591translocation1nstd200human GRCh37 chr6: 37,661,734-37,661,734 , GRCh37 chr6: 37,662,631-37,662,631 , GRCh38.p12 chr6: 37,693,958-37,693,958 , GRCh38.p12 chr6: 37,694,855-37,694,855 MDGA1
    nsv5328273translocation1nstd204human GRCh38.p13 chr6: 37,677,627-37,677,627 , GRCh38.p13 chr6: 37,675,766-37,675,766 , GRCh37.p13 chr6: 37,643,542-37,643,542 , GRCh37.p13 chr6: 37,645,403-37,645,403 MDGA1
    nsv5319917copy number variation1nstd204human GRCh38.p13 chr6: 37,674,893-37,677,655 , GRCh37.p13 chr6: 37,642,669-37,645,431 MDGA1
    nsv5237017copy number variation1nstd204human GRCh38.p13 chr6: 37,674,901-37,677,600 , GRCh37.p13 chr6: 37,642,677-37,645,376 MDGA1
    nsv5222559copy number variation1nstd204human GRCh38.p13 chr6: 37,675,234-37,677,883 , GRCh37.p13 chr6: 37,643,010-37,645,659 MDGA1
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4940965copy number variation1nstd200human GRCh38 chr6: 37,690,685-37,693,709 , GRCh37.p13 chr6: 37,658,461-37,661,485 MDGA1
    nsv4940964copy number variation1nstd200human GRCh38 chr6: 37,674,893-37,677,655 , GRCh37.p13 chr6: 37,642,669-37,645,431 MDGA1
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 more genes
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