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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112692copy number variation1nstd102humanPathogenic GRCh38 chr7: 42,076,258-42,077,316 , GRCh37 chr7: 42,115,857-42,116,915 GLI3
    nsv5954416insertion1nstd209human GRCh38 chr7: 42,182,662-42,182,662 , GRCh37.p13 chr7: 42,222,261-42,222,261 GLI3
    nsv5914800copy number variation1nstd209human GRCh38 chr7: 42,204,139-42,204,227 , GRCh37.p13 chr7: 42,243,738-42,243,826 GLI3
    nsv5908557copy number variation1nstd209human GRCh38 chr7: 42,203,096-42,203,170 , GRCh37.p13 chr7: 42,242,695-42,242,769 GLI3
    nsv5715657mobile element insertion1nstd211human GRCh38 chr7: 42,007,338-42,007,338 , GRCh37.p13 chr7: 42,046,937-42,046,937 GLI3
    nsv5689317mobile element insertion2nstd211human GRCh38 chr7: 41,968,804-41,968,804 , GRCh37.p13 chr7: 42,008,403-42,008,403 GLI3
    nsv5683811mobile element insertion1nstd211human GRCh38 chr7: 41,971,103-41,971,103 , GRCh37.p13 chr7: 42,010,702-42,010,702 GLI3
    nsv5674032copy number variation1nstd102humanPathogenic GRCh37 chr7: 42,187,805-42,262,872 , GRCh38.p12 chr7: 42,148,206-42,223,273 GLI3
    nsv5673794copy number variation1nstd102humanPathogenic GRCh37 chr7: 42,116,331-42,188,087 , GRCh38.p12 chr7: 42,076,732-42,148,488 GLI3, HMGN2P30
    nsv5636392insertion1nstd207human GRCh38 chr7: 42,182,664-42,182,664 , GRCh37.p13 chr7: 42,222,263-42,222,263 GLI3
    nsv5563974mobile element insertion1nstd206human GRCh38 chr7: 42,007,338-42,007,389 , GRCh37.p13 chr7: 42,046,937-42,046,988 GLI3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491701copy number variation1nstd206human GRCh38 chr7: 42,216,995-42,217,085 , GRCh37.p13 chr7: 42,256,594-42,256,684 GLI3
    nsv5490938copy number variation1nstd206human GRCh38 chr7: 41,968,855-41,968,987 , GRCh37.p13 chr7: 42,008,454-42,008,586 GLI3
    nsv5489807copy number variation1nstd206human GRCh38 chr7: 42,050,897-42,053,147 , GRCh37.p13 chr7: 42,090,496-42,092,746 GLI3
    nsv5487933copy number variation1nstd206human GRCh38 chr7: 42,199,874-42,201,900 , GRCh37.p13 chr7: 42,239,473-42,241,499 GLI3
    nsv5485645copy number variation1nstd206human GRCh38 chr7: 42,096,077-42,129,328 , GRCh37.p13 chr7: 42,135,676-42,168,927 GLI3, HMGN2P30
    nsv5484240copy number variation1nstd206human GRCh38 chr7: 42,043,385-42,043,750 , GRCh37.p13 chr7: 42,082,984-42,083,349 GLI3
    nsv5483666copy number variation1nstd206human GRCh38 chr7: 42,207,267-42,210,791 , GRCh37.p13 chr7: 42,246,866-42,250,390 GLI3
    nsv5479183copy number variation1nstd206human GRCh38 chr7: 42,182,883-42,182,993 , GRCh37.p13 chr7: 42,222,482-42,222,592 GLI3
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