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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6915849copy number variation1nstd229human GRCh38 chr11: 36,279,082-36,279,248 , GRCh37.p13 chr11: 36,300,632-36,300,798 COMMD9
    nsv6913781copy number variation1nstd229human GRCh38 chr11: 34,168,221-36,836,658 , GRCh37.p13 chr11: 34,189,768-36,858,208 TRAF6, LOC100422241, 39 more genes
    nsv6913461copy number variation1nstd229human GRCh38 chr11: 36,200,200-36,302,574 , GRCh37.p13 chr11: 36,221,750-36,324,124 COMMD9, PRR5L, 1 more genes
    nsv6908350copy number variation1nstd229human GRCh38 chr11: 36,267,353-36,275,134 , GRCh37.p13 chr11: 36,288,903-36,296,684 COMMD9
    nsv6904806copy number variation1nstd229human GRCh38 chr11: 36,268,317-36,299,192 , GRCh37.p13 chr11: 36,289,867-36,320,742 COMMD9, PRR5L
    nsv6902738copy number variation1nstd229human GRCh38 chr11: 36,269,259-36,272,128 , GRCh37.p13 chr11: 36,290,809-36,293,678 COMMD9
    nsv6899992copy number variation1nstd229human GRCh38 chr11: 36,267,144-36,293,822 , GRCh37.p13 chr11: 36,288,694-36,315,372 COMMD9
    nsv6899421copy number variation1nstd229human GRCh38 chr11: 36,270,037-36,273,287 , GRCh37.p13 chr11: 36,291,587-36,294,837 COMMD9
    nsv6899013copy number variation1nstd229human GRCh38 chr11: 36,247,989-36,402,588 , GRCh37.p13 chr11: 36,269,539-36,424,138 PRR5L, COMMD9
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 more genes
    nsv6468584copy number variation1nstd223human GRCh38 chr11: 36,200,200-36,302,574 , GRCh37.p13 chr11: 36,221,750-36,324,124 LDLRAD3, PRR5L, 1 more genes
    nsv6456232copy number variation1nstd223human GRCh38 chr11: 36,270,001-36,272,100 , GRCh37.p13 chr11: 36,291,551-36,293,650 COMMD9
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6096935insertion1nstd212human GRCh38 chr11: 36,287,302-36,287,302 , GRCh37.p13 chr11: 36,308,852-36,308,852 COMMD9
    nsv6095601insertion1nstd212human GRCh38 chr11: 36,287,062-36,287,062 , GRCh37.p13 chr11: 36,308,612-36,308,612 COMMD9
    nsv6023385copy number variation1nstd212human GRCh38 chr11: 36,287,118-36,287,477 , GRCh37.p13 chr11: 36,308,668-36,309,027 COMMD9
    nsv5663527insertion1nstd207human GRCh38 chr11: 36,287,335-36,287,335 , GRCh37.p13 chr11: 36,308,885-36,308,885 COMMD9
    nsv5662196insertion2nstd207human GRCh38 chr11: 36,287,046-36,287,046 , GRCh37.p13 chr11: 36,308,596-36,308,596 COMMD9
    nsv5649269insertion1nstd207human GRCh38 chr11: 36,287,054-36,287,054 , GRCh37.p13 chr11: 36,308,604-36,308,604 COMMD9
    nsv5645891insertion2nstd207human GRCh38 chr11: 36,287,440-36,287,440 , GRCh37.p13 chr11: 36,308,990-36,308,990 COMMD9
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