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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126328insertion1nstd186human GRCh37 chr11: 66,365,934-66,365,934 , GRCh38.p12 chr11: 66,598,463-66,598,463 CCS
    nsv5655050insertion1nstd207human GRCh38 chr11: 66,598,463-66,598,463 , GRCh37.p13 chr11: 66,365,934-66,365,934 CCS
    nsv5555397sequence alteration1nstd206human GRCh38 chr11: 66,593,877-66,594,706 , GRCh37.p13 chr11: 66,361,348-66,362,177 CCS
    nsv5543926insertion1nstd206human GRCh38 chr11: 66,598,463-66,598,463 , GRCh37.p13 chr11: 66,365,934-66,365,934 CCS
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5139240mobile element insertion1nstd203human GRCh38 chr11: 66,598,472-66,598,489 , GRCh37.p13 chr11: 66,365,943-66,365,960 CCS
    nsv5137825mobile element insertion1nstd203human GRCh38 chr11: 66,598,453-66,598,489 , GRCh37.p13 chr11: 66,365,924-66,365,960 CCS
    nsv5137756mobile element insertion1nstd203human GRCh38 chr11: 66,598,480-66,598,489 , GRCh37.p13 chr11: 66,365,951-66,365,960 CCS
    nsv5136984mobile element insertion1nstd203human GRCh38 chr11: 66,598,465-66,598,489 , GRCh37.p13 chr11: 66,365,936-66,365,960 CCS
    nsv5136781mobile element insertion1nstd203human GRCh38 chr11: 66,598,467-66,598,489 , GRCh37.p13 chr11: 66,365,938-66,365,960 CCS
    nsv5136287mobile element insertion1nstd203human GRCh38 chr11: 66,598,001-66,598,008 , GRCh37.p13 chr11: 66,365,472-66,365,479 CCS
    nsv5135293mobile element insertion1nstd203human GRCh38 chr11: 66,598,474-66,598,489 , GRCh37.p13 chr11: 66,365,945-66,365,960 CCS
    nsv5134731mobile element insertion1nstd203human GRCh38 chr11: 66,598,478-66,598,489 , GRCh37.p13 chr11: 66,365,949-66,365,960 CCS
    nsv5134423mobile element insertion1nstd203human GRCh38 chr11: 66,598,484-66,598,489 , GRCh37.p13 chr11: 66,365,955-66,365,960 CCS
    nsv5133873mobile element insertion1nstd203human GRCh38 chr11: 66,598,446-66,598,489 , GRCh37.p13 chr11: 66,365,917-66,365,960 CCS
    nsv5132208mobile element insertion1nstd203human GRCh38 chr11: 66,598,483-66,598,489 , GRCh37.p13 chr11: 66,365,954-66,365,960 CCS
    nsv5131936mobile element insertion1nstd203human GRCh38 chr11: 66,598,463-66,598,489 , GRCh37.p13 chr11: 66,365,934-66,365,960 CCS
    nsv5131214mobile element insertion1nstd203human GRCh38 chr11: 66,598,466-66,598,489 , GRCh37.p13 chr11: 66,365,937-66,365,960 CCS
    nsv5130583mobile element insertion1nstd203human GRCh38 chr11: 66,598,489-66,598,504 , GRCh37.p13 chr11: 66,365,960-66,365,975 CCS
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