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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147791copy number variation1nstd232human GRCh37.p13 chr11: 10,820,971-10,821,097 , GRCh38.p12 chr11: 10,799,424-10,799,550 EIF4G2, SNORD97
    nsv7147068copy number variation1nstd232human GRCh37.p13 chr11: 10,825,750-10,825,832 , GRCh38.p12 chr11: 10,804,203-10,804,285 EIF4G2
    nsv7145893insertion1nstd232human GRCh37.p13 chr11: 10,824,844-10,824,844 , GRCh38.p12 chr11: 10,803,297-10,803,297 EIF4G2
    nsv7142794copy number variation1nstd232human GRCh37.p13 chr11: 10,821,894-10,821,976 , GRCh38.p12 chr11: 10,800,347-10,800,429 EIF4G2, SNORD97
    nsv7142651copy number variation1nstd232human GRCh37.p13 chr11: 10,823,753-10,823,836 , GRCh38.p12 chr11: 10,802,206-10,802,289 EIF4G2
    nsv7142088copy number variation1nstd232human GRCh37.p13 chr11: 10,825,597-10,825,682 , GRCh38.p12 chr11: 10,804,050-10,804,135 EIF4G2
    nsv7139870copy number variation1nstd232human GRCh37.p13 chr11: 10,822,193-10,822,275 , GRCh38.p12 chr11: 10,800,646-10,800,728 EIF4G2, SNORD97
    nsv7139376copy number variation1nstd232human GRCh37.p13 chr11: 10,824,674-10,824,755 , GRCh38.p12 chr11: 10,803,127-10,803,208 EIF4G2
    nsv7138648copy number variation1nstd232human GRCh37.p13 chr11: 10,820,659-10,820,757 , GRCh38.p12 chr11: 10,799,112-10,799,210 EIF4G2
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6903709copy number variation1nstd229human GRCh38 chr11: 10,805,656-10,805,747 , GRCh37.p13 chr11: 10,827,203-10,827,294 EIF4G2
    nsv6902202copy number variation1nstd229human GRCh38 chr11: 10,809,441-11,211,128 , GRCh37.p13 chr11: 10,830,988-11,232,675 EIF4G2, ZBED5-AS1, 8 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6281198insertion3nstd214human GRCh38 chr11: 10,802,029-10,802,029 , GRCh37.p13 chr11: 10,823,576-10,823,576 SNORD97, EIF4G2
    nsv6132006copy number variation1nstd213human GRCh37 chr11: 10,720,000-11,190,001 , GRCh38.p12 chr11: 10,698,453-11,168,454 EIF4G2, CTR9, 9 more genes
    nsv6091880insertion1nstd212human GRCh38 chr11: 10,802,029-10,802,029 , GRCh37.p13 chr11: 10,823,576-10,823,576 EIF4G2, SNORD97
    nsv6025788copy number variation1nstd212human GRCh38 chr11: 10,805,656-10,805,747 , GRCh37.p13 chr11: 10,827,203-10,827,294 EIF4G2
    nsv5974165insertion1nstd209human GRCh38 chr11: 10,802,029-10,802,029 , GRCh37.p13 chr11: 10,823,576-10,823,576 EIF4G2, SNORD97
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