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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901448copy number variation1nstd209human GRCh38 chr6: 41,643,518-41,643,589 , GRCh37.p13 chr6: 41,611,256-41,611,327 MDFI
    nsv5895958copy number variation1nstd209human GRCh38 chr6: 41,651,096-41,651,544 , GRCh37.p13 chr6: 41,618,834-41,619,282 MDFI
    nsv5679695mobile element insertion1nstd211human GRCh38 chr6: 41,651,545-41,651,545 , GRCh37.p13 chr6: 41,619,283-41,619,283 MDFI
    nsv5640336insertion1nstd207human GRCh38 chr6: 41,639,230-41,639,230 , GRCh37.p13 chr6: 41,606,968-41,606,968 MDFI
    nsv5625942insertion1nstd207human GRCh38 chr6: 41,643,572-41,643,572 , GRCh37.p13 chr6: 41,611,310-41,611,310 MDFI
    nsv5572385copy number variation1nstd207human GRCh38 chr6: 41,651,096-41,651,544 , GRCh37.p13 chr6: 41,618,834-41,619,282 MDFI
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5473862copy number variation1nstd206human GRCh38 chr6: 41,654,425-41,654,493 , GRCh37.p13 chr6: 41,622,163-41,622,231 MDFI
    nsv5454840copy number variation1nstd206human GRCh38 chr6: 41,651,097-41,651,545 , GRCh37.p13 chr6: 41,618,835-41,619,283 MDFI
    nsv5303136copy number variation1nstd204human GRCh38.p13 chr6: 41,651,097-41,651,545 , GRCh37.p13 chr6: 41,618,835-41,619,283 MDFI
    nsv5233386copy number variation1nstd204human GRCh38.p13 chr6: 41,651,101-41,651,500 , GRCh37.p13 chr6: 41,618,839-41,619,238 MDFI
    nsv4941074copy number variation1nstd200human GRCh38 chr6: 41,651,986-41,652,213 , GRCh37.p13 chr6: 41,619,724-41,619,951 MDFI
    nsv4941073copy number variation1nstd200human GRCh38 chr6: 41,651,097-41,651,545 , GRCh37.p13 chr6: 41,618,835-41,619,283 MDFI
    nsv4934662copy number variation1nstd200human GRCh38 chr6: 41,581,362-41,647,014 , GRCh37.p13 chr6: 41,549,100-41,614,752 MDFI, FOXP4, 1 more genes
    nsv4828663copy number variation1nstd200human GRCh37 chr6: 41,549,100-41,614,752 , GRCh38.p12 chr6: 41,581,362-41,647,014 MIR4641, FOXP4, 1 more genes
    nsv4816155copy number variation1nstd200human GRCh37 chr6: 41,619,724-41,619,951 , GRCh38.p12 chr6: 41,651,986-41,652,213 MDFI
    nsv4816154copy number variation1nstd200human GRCh37 chr6: 41,618,835-41,619,283 , GRCh38.p12 chr6: 41,651,097-41,651,545 MDFI
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4745631copy number variation1nstd199human GRCh37 chr6: 41,598,679-41,609,848 , GRCh38.p12 chr6: 41,630,941-41,642,110 MDFI
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