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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909756copy number variation1nstd102humanBenign GRCh37 chr16: 30,376,486-30,382,642 , GRCh38.p12 chr16: 30,365,165-30,371,321 MYL11, TBC1D10B
    nsv3904808copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,872-30,385,953 , GRCh38.p12 chr16: 30,369,551-30,374,632 MYL11, TBC1D10B
    nsv3900245copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,872-30,385,837 , GRCh38.p12 chr16: 30,369,551-30,374,516 MYL11, TBC1D10B
    nsv3897236copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,872-30,382,642 , GRCh38.p12 chr16: 30,369,551-30,371,321 MYL11, TBC1D10B
    nsv3902248copy number variation1nstd102humanBenign GRCh37 chr16: 30,381,072-30,382,642 , GRCh38.p12 chr16: 30,369,751-30,371,321 MYL11, TBC1D10B
    nsv3900067copy number variation1nstd102humanBenign GRCh37 chr16: 30,381,378-30,382,642 , GRCh38.p12 chr16: 30,370,057-30,371,321 MYL11, TBC1D10B
    nsv3899279copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,486-30,381,735 , GRCh38.p12 chr16: 30,369,165-30,370,414 MYL11, TBC1D10B
    nsv3901369copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,486-30,381,633 , GRCh38.p12 chr16: 30,369,165-30,370,312 MYL11, TBC1D10B
    nsv3891158copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,872-30,381,735 , GRCh38.p12 chr16: 30,369,551-30,370,414 MYL11, TBC1D10B
    nsv3906549copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,970-30,381,735 , GRCh38.p12 chr16: 30,369,649-30,370,414 MYL11, TBC1D10B
    nsv3892455copy number variation1nstd102humanBenign GRCh37 chr16: 30,380,872-30,381,633 , GRCh38.p12 chr16: 30,369,551-30,370,312 MYL11, TBC1D10B
    nsv3906899copy number variation1nstd102humanBenign GRCh37 chr16: 30,381,174-30,381,735 , GRCh38.p12 chr16: 30,369,853-30,370,414 MYL11, TBC1D10B
    nsv3897306copy number variation1nstd102humanBenign GRCh37 chr16: 30,376,269-30,420,851 , GRCh38.p12 chr16: 30,364,948-30,409,530 MYL11, ZNF771, 3 more genes
    nsv1398149copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,386,180-30,390,806 , GRCh38.p12 chr16: 30,374,859-30,379,485 MYL11, SEPTIN1, 1 more genes
    nsv3905855copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846 MYL11, LOC107984874, 217 more genes
    nsv3911651copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,500,284-30,610,734 , GRCh38 chr16: 29,581,462-30,691,912 , GRCh37 chr16: 29,592,783-30,703,233 MYL11, PPP4C, 71 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 MYL11, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 MYL11, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 MYL11, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 MYL11, PRSS53, 1868 more genes
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