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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980448copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,960,991-88,961,138 , GRCh38.p12 chr11: 89,227,823-89,227,970 TYR
    nsv5980268insertion1nstd209human GRCh38 chr11: 89,175,769-89,175,769 , GRCh37.p13 chr11: 88,908,937-88,908,937 , TYR
    nsv5968431insertion1nstd209human GRCh38 chr11: 89,288,894-89,288,894 , GRCh37.p13 chr11: 89,022,062-89,022,062 , TYR
    nsv5927081copy number variation1nstd209human GRCh38 chr11: 89,264,409-89,270,052 , GRCh37.p13 chr11: 88,997,577-89,003,220 , TYR
    nsv5923781copy number variation1nstd209human GRCh38 chr11: 89,231,314-89,234,761 , GRCh37.p13 chr11: 88,964,482-88,967,929 , TYR
    nsv5919053copy number variation1nstd209human GRCh38 chr11: 89,175,977-89,176,039 , GRCh37.p13 chr11: 88,909,145-88,909,207 , TYR
    nsv5916559copy number variation1nstd209human GRCh38 chr11: 89,184,168-89,184,246 , GRCh37.p13 chr11: 88,917,336-88,917,414 , TYR
    nsv5910300copy number variation1nstd209human GRCh38 chr11: 89,174,074-89,539,687 , GRCh37.p13 chr11: 88,907,242-89,272,855 , NOX4, 2 more genes
    nsv5909705copy number variation1nstd209human GRCh38 chr11: 89,228,889-89,231,063 , GRCh37.p13 chr11: 88,962,057-88,964,231 , TYR
    nsv5865783copy number variation1nstd209human GRCh38 chr11: 89,234,787-89,264,306 , GRCh37.p13 chr11: 88,967,955-88,997,474 , TYR
    nsv5864846copy number variation2nstd209human GRCh38 chr11: 89,265,626-89,270,265 , GRCh37.p13 chr11: 88,998,794-89,003,433 , TYR
    nsv5858787copy number variation1nstd209human GRCh38 chr11: 89,234,349-89,237,288 , GRCh37.p13 chr11: 88,967,517-88,970,456 , TYR
    nsv5858165copy number variation1nstd209human GRCh38 chr11: 89,174,031-89,224,669 , GRCh37.p13 chr11: 88,907,199-88,957,837 , TYR
    nsv5857172copy number variation2nstd209human GRCh38 chr11: 89,228,849-89,231,148 , GRCh37.p13 chr11: 88,962,017-88,964,316 , TYR
    nsv5853760copy number variation1nstd209human GRCh38 chr11: 89,224,624-89,232,398 , GRCh37.p13 chr11: 88,957,792-88,965,566 , TYR
    nsv5851687copy number variation1nstd209human GRCh38 chr11: 89,231,349-89,234,748 , GRCh37.p13 chr11: 88,964,517-88,967,916 , TYR
    nsv5851104copy number variation1nstd209human GRCh38 chr11: 89,225,749-89,229,848 , GRCh37.p13 chr11: 88,958,917-88,963,016 , TYR
    nsv5726667mobile element insertion1nstd211human GRCh38 chr11: 89,258,051-89,258,051 , GRCh37.p13 chr11: 88,991,219-88,991,219 , TYR
    nsv5724250mobile element insertion1nstd211human GRCh38 chr11: 89,293,806-89,293,806 , GRCh37.p13 chr11: 89,026,974-89,026,974 TYR, CBX3P7
    nsv5712627mobile element insertion1nstd211human GRCh38 chr11: 89,187,833-89,187,833 , GRCh37.p13 chr11: 88,921,001-88,921,001 , TYR
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