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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968639insertion1nstd209human GRCh38 chr11: 31,581,473-31,581,473 , GRCh37.p13 chr11: 31,603,020-31,603,020 ELP4
    nsv5927294copy number variation1nstd209human GRCh38 chr11: 31,675,993-31,679,627 , GRCh37.p13 chr11: 31,697,541-31,701,175 ELP4
    nsv5922604copy number variation1nstd209human GRCh38 chr11: 31,544,883-31,549,073 , GRCh37.p13 chr11: 31,566,430-31,570,620 ELP4
    nsv5918153copy number variation1nstd209human GRCh38 chr11: 31,590,762-31,593,475 , GRCh37.p13 chr11: 31,612,309-31,615,022 ELP4
    nsv5916692copy number variation1nstd209human GRCh38 chr11: 31,595,822-31,598,565 , GRCh37.p13 chr11: 31,617,369-31,620,112 ELP4
    nsv5863348copy number variation1nstd209human GRCh38 chr11: 31,512,714-31,516,525 , GRCh37.p13 chr11: 31,534,261-31,538,072 ELP4
    nsv5860503copy number variation1nstd209human GRCh38 chr11: 31,595,933-31,598,332 , GRCh37.p13 chr11: 31,617,480-31,619,879 ELP4
    nsv5859459copy number variation2nstd209human GRCh38 chr11: 31,545,152-31,547,145 , GRCh37.p13 chr11: 31,566,699-31,568,692 ELP4
    nsv5857946copy number variation1nstd209human GRCh38 chr11: 31,590,965-31,592,264 , GRCh37.p13 chr11: 31,612,512-31,613,811 ELP4
    nsv5857806copy number variation1nstd209human GRCh38 chr11: 31,544,852-31,549,020 , GRCh37.p13 chr11: 31,566,399-31,570,567 ELP4
    nsv5857528copy number variation1nstd209human GRCh38 chr11: 31,675,921-31,679,667 , GRCh37.p13 chr11: 31,697,469-31,701,215 ELP4
    nsv5702814mobile element insertion1nstd211human GRCh38 chr11: 31,788,862-31,788,862 , GRCh37.p13 chr11: 31,810,410-31,810,410 PAX6, ELP4
    nsv5701448mobile element insertion1nstd211human GRCh38 chr11: 31,591,432-31,591,432 , GRCh37.p13 chr11: 31,612,979-31,612,979 ELP4
    nsv5699274mobile element insertion1nstd211human GRCh38 chr11: 31,672,353-31,672,353 , GRCh37.p13 chr11: 31,693,901-31,693,901 ELP4
    nsv5697357mobile element insertion2nstd211human GRCh38 chr11: 31,663,232-31,663,232 , GRCh37.p13 chr11: 31,684,780-31,684,780 ELP4
    nsv5672779copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,804,921-31,816,377 , GRCh38.p12 chr11: 31,783,373-31,794,829 PAX6, ELP4
    nsv5672630copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,284,590-31,824,402 , GRCh38.p12 chr11: 31,263,043-31,802,854 PAX6, ELP4, 4 more genes
    nsv5654410insertion1nstd207human GRCh38 chr11: 31,560,684-31,560,684 , GRCh37.p13 chr11: 31,582,231-31,582,231 ELP4
    nsv5512981copy number variation1nstd206human GRCh38 chr11: 31,685,453-31,689,361 , GRCh37.p13 chr11: 31,707,001-31,710,909 ELP4
    nsv5508800copy number variation1nstd206human GRCh38 chr11: 31,715,986-31,716,048 , GRCh37.p13 chr11: 31,737,534-31,737,596 ELP4
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