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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978598insertion1nstd209human GRCh38 chr11: 47,558,687-47,558,687 , GRCh37.p13 chr11: 47,580,239-47,580,239 CELF1
    nsv5972141insertion1nstd209human GRCh38 chr11: 47,489,935-47,489,935 , GRCh37.p13 chr11: 47,511,487-47,511,487 CELF1
    nsv5915938copy number variation1nstd209human GRCh38 chr11: 47,558,537-47,558,588 , GRCh37.p13 chr11: 47,580,089-47,580,140 CELF1
    nsv5913980copy number variation1nstd209human GRCh38 chr11: 47,541,686-47,541,785 , GRCh37.p13 chr11: 47,563,238-47,563,337 CELF1
    nsv5908261copy number variation1nstd209human GRCh38 chr11: 47,504,552-47,506,401 , GRCh37.p13 chr11: 47,526,104-47,527,953 CELF1
    nsv5848428copy number variation1nstd209human GRCh38 chr11: 47,504,531-47,506,430 , GRCh37.p13 chr11: 47,526,083-47,527,982 CELF1
    nsv5696539mobile element insertion1nstd211human GRCh38 chr11: 47,508,572-47,508,572 , GRCh37.p13 chr11: 47,530,124-47,530,124 CELF1
    nsv5655548insertion1nstd207human GRCh38 chr11: 47,557,553-47,557,553 , GRCh37.p13 chr11: 47,579,105-47,579,105 CELF1, RN7SL652P
    nsv5595527copy number variation1nstd207human GRCh38 chr11: 47,541,717-47,541,792 , GRCh37.p13 chr11: 47,563,269-47,563,344 CELF1
    nsv5559589sequence alteration1nstd206human GRCh38 chr11: 47,500,647-47,504,854 , GRCh37.p13 chr11: 47,522,199-47,526,406 CELF1
    nsv5548740insertion1nstd206human GRCh38 chr11: 47,558,728-47,558,738 , GRCh37.p13 chr11: 47,580,280-47,580,290 CELF1
    nsv5504444copy number variation1nstd206human GRCh38 chr11: 47,500,000-47,505,000 , GRCh37.p13 chr11: 47,521,552-47,526,552 CELF1
    nsv5501400copy number variation1nstd206human GRCh38 chr11: 47,541,686-47,541,772 , GRCh37.p13 chr11: 47,563,238-47,563,324 CELF1
    nsv5500679copy number variation1nstd206human GRCh38 chr11: 47,504,556-47,506,394 , GRCh37.p13 chr11: 47,526,108-47,527,946 CELF1
    nsv5495214copy number variation1nstd206human GRCh38 chr11: 47,562,483-47,564,723 , GRCh37.p13 chr11: 47,584,035-47,586,275 CELF1, PTPMT1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5373558translocation1nstd200human GRCh38 chr11: 47,504,855-47,504,855 , GRCh38 chr11: 47,502,916-47,502,916 , GRCh37.p13 chr11: 47,524,468-47,524,468 , GRCh37.p13 chr11: 47,526,407-47,526,407 CELF1
    nsv5373557translocation1nstd200human GRCh38 chr11: 47,500,647-47,500,647 , GRCh38 chr11: 47,503,303-47,503,303 , GRCh37.p13 chr11: 47,522,199-47,522,199 , GRCh37.p13 chr11: 47,524,855-47,524,855 CELF1
    nsv5339815translocation1nstd200human GRCh37 chr11: 47,485,845-47,485,845 , GRCh37 chr11: 47,485,779-47,485,779 , GRCh38.p12 chr11: 47,464,227-47,464,227 , GRCh38.p12 chr11: 47,464,293-47,464,293 CELF1
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