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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
    nsv7097824copy number variation1nstd102humanUncertain significance GRCh37 chr6: 393,153-393,388 , GRCh38.p12 chr6: 393,153-393,388 IRF4
    nsv7097430copy number variation1nstd102humanUncertain significance GRCh37 chr6: 393,153-395,027 , GRCh38.p12 chr6: 393,153-395,027 IRF4
    nsv7093358copy number variation1nstd102humanUncertain significance GRCh37 chr6: 160,000-820,000 , GRCh38.p12 chr6: 160,000-820,000 EXOC2, LOC105374873, 7 more genes
    nsv7053468inversion1nstd229human GRCh38 chr6: 285,653-485,550 , GRCh37.p13 chr6: 285,653-485,550 EXOC2, DUSP22, 1 more genes
    nsv7053420inversion1nstd229human GRCh38 chr6: 196,722-448,065 , GRCh37.p13 chr6: 196,722-448,065 IRF4, LOC105374870, 2 more genes
    nsv7044237inversion1nstd229human GRCh38 chr6: 299,246-471,853 , GRCh37.p13 chr6: 299,246-471,853 IRF4, DUSP22
    nsv7038280inversion1nstd229human GRCh38 chr6: 208,989-447,796 , GRCh37.p13 chr6: 208,989-447,796 IRF4, LOC105374870, 1 more genes
    nsv6790842copy number variation1nstd229human GRCh38 chr6: 400,097-421,569 , GRCh37.p13 chr6: 400,097-421,569 IRF4
    nsv6790720copy number variation1nstd229human GRCh38 chr6: 403,804-851,832 , GRCh37.p13 chr6: 403,804-851,832 MARK2P18, LOC105374873, 3 more genes
    nsv6783501copy number variation1nstd229human GRCh38 chr6: 400,854-495,512 , GRCh37.p13 chr6: 400,854-495,512 IRF4, EXOC2
    nsv6781236copy number variation1nstd229human GRCh38 chr6: 395,739-487,335 , GRCh37.p13 chr6: 395,739-487,335 IRF4, EXOC2
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6636561copy number variation1nstd102humanUncertain significance GRCh37 chr6: 381,086-1,144,691 , GRCh38.p12 chr6: 381,086-1,144,456 LOC101927691, HUS1B, 5 more genes
    nsv6631498copy number variation1nstd224human GRCh37 chr6: 410,493-421,317 , GRCh38.p12 chr6: 410,493-421,317 IRF4
    nsv6631412copy number variation1nstd224human GRCh37 chr6: 394,867-776,262 , GRCh38.p12 chr6: 394,867-776,262 IRF4, HUS1B, 3 more genes
    nsv6630676copy number variation1nstd224human GRCh37 chr6: 150,279-848,949 , GRCh38.p12 chr6: 150,279-848,949 IRF4, EXOC2, 7 more genes
    nsv6574826inversion1nstd223human GRCh38 chr6: 196,714-448,068 , GRCh37.p13 chr6: 196,714-448,068 IRF4, DUSP22, 2 more genes
    nsv6412355copy number variation1nstd223human GRCh38 chr6: 253,801-453,800 , GRCh37.p13 chr6: 253,801-453,800 DUSP22, IRF4
    nsv6411993copy number variation1nstd223human GRCh38 chr6: 253,301-458,900 , GRCh37.p13 chr6: 253,301-458,900 IRF4, DUSP22
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