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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925576copy number variation1nstd209human GRCh38 chr6: 169,771,709-169,771,836 , GRCh37.p13 chr6: 170,171,805-170,171,932 ERMARD
    nsv5922362copy number variation1nstd209human GRCh38 chr6: 169,765,858-169,766,001 , GRCh37.p13 chr6: 170,165,954-170,166,097 ERMARD
    nsv5631220insertion1nstd207human GRCh38 chr6: 169,771,709-169,771,709 , GRCh37.p13 chr6: 170,171,805-170,171,805 ERMARD
    nsv5577838copy number variation1nstd207human GRCh38 chr6: 169,765,858-169,766,001 , GRCh37.p13 chr6: 170,165,954-170,166,097 ERMARD
    nsv5552611insertion1nstd206human GRCh38 chr6: 169,751,830-169,751,844 , GRCh37.p13 chr6: 170,151,926-170,151,940 DYNLT2, ERMARD
    nsv5457502copy number variation1nstd206human GRCh38 chr6: 169,758,292-169,758,377 , GRCh37.p13 chr6: 170,158,388-170,158,473 ERMARD
    nsv5456133copy number variation1nstd206human GRCh38 chr6: 169,771,709-169,771,837 , GRCh37.p13 chr6: 170,171,805-170,171,933 ERMARD
    nsv5302577copy number variation1nstd204human GRCh38.p13 chr6: 169,764,092-169,770,372 , GRCh37.p13 chr6: 170,164,188-170,170,468 ERMARD
    nsv5223080copy number variation1nstd204human GRCh38.p13 chr6: 169,764,101-169,770,200 , GRCh37.p13 chr6: 170,164,197-170,170,296 ERMARD
    nsv5222181copy number variation1nstd204human GRCh38.p13 chr6: 169,764,068-169,770,363 , GRCh37.p13 chr6: 170,164,164-170,170,459 ERMARD
    nsv5119434mobile element insertion1nstd203human GRCh38 chr6: 169,754,991-169,755,003 , GRCh37.p13 chr6: 170,155,087-170,155,099 ERMARD
    nsv5103891mobile element insertion1nstd203human GRCh38 chr6: 169,768,983-169,768,997 , GRCh37.p13 chr6: 170,169,079-170,169,093 ERMARD
    nsv4966054copy number variation1nstd200human GRCh38 chr6: 169,764,115-169,770,343 , GRCh37.p13 chr6: 170,164,211-170,170,439 ERMARD
    nsv4966027copy number variation1nstd200human GRCh38 chr6: 169,180,752-170,050,020 , GRCh37.p13 chr6: 169,580,847-170,365,244 , LOC100131532, 17 more genes
    nsv4953150copy number variation1nstd200human GRCh38 chr6: 169,761,781-169,771,383 , GRCh37.p13 chr6: 170,161,877-170,171,479 ERMARD
    nsv4818146copy number variation1nstd200human GRCh37 chr6: 170,164,211-170,170,439 , GRCh38.p12 chr6: 169,764,115-169,770,343 , GRCh38.p12 chr6|NT_187552.1: 39,317-45,545 ERMARD
    nsv4748637copy number variation1nstd199human GRCh37 chr6: 170,165,965-170,166,109 , GRCh38.p12 chr6|NT_187552.1: 41,071-41,215 , GRCh38.p12 chr6: 169,765,869-169,766,013 ERMARD
    nsv4748193copy number variation1nstd199human GRCh37 chr6: 170,181,967-170,182,161 , GRCh38.p12 chr6: 169,781,871-169,782,065 , GRCh38.p12 chr6|NT_187552.1: 57,073-57,267 ERMARD
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4729261copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,580,012-170,919,482 , GRCh38.p12 chr6: 167,166,524-170,610,394 LOC107986549, AFDN, 81 more genes
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