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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3894818copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,959,766-34,960,308 , GRCh38.p12 chr20: 36,331,363-36,331,905 DLGAP4
    nsv3899003copy number variation1nstd102humanLikely benign GRCh37 chr18: 4,196,265-4,249,393 , GRCh38.p12 chr18: 4,196,265-4,249,393 DLGAP1
    nsv3878911copy number variation1nstd102humanBenign GRCh37 chr1: 155,662,247-155,677,223 , GRCh38.p12 chr1: 155,692,456-155,707,432 DAP3
    nsv3883402copy number variation1nstd102humanBenign GRCh37 chr1: 155,662,247-155,676,492 , GRCh38.p12 chr1: 155,692,456-155,706,701 DAP3
    nsv3876547copy number variation1nstd102humanBenign GRCh37 chr5: 10,752,315-10,761,880 , GRCh38.p12 chr5: 10,752,203-10,761,768 DAP
    nsv3898530copy number variation1nstd102humanBenign GRCh37 chr18: 4,328,652-4,335,455 , GRCh38.p12 chr18: 4,328,652-4,335,455 DLGAP1
    nsv3907067copy number variation1nstd102humanBenign GRCh37 chr18: 4,157,461-4,164,141 , GRCh38.p12 chr18: 4,157,461-4,164,141 DLGAP1
    nsv3880035copy number variation1nstd102humanBenign GRCh37 chr1: 155,662,247-155,664,439 , GRCh38.p12 chr1: 155,692,456-155,694,648 DAP3
    nsv3887538copy number variation1nstd102humanBenign GRCh37 chr1: 155,662,247-155,664,301 , GRCh38.p12 chr1: 155,692,456-155,694,510 DAP3
    nsv3895974copy number variation1nstd102humanBenign GRCh37 chr18: 3,635,577-3,637,344 , GRCh38.p12 chr18: 3,635,578-3,637,345 DLGAP1
    nsv3884054copy number variation1nstd102humanBenign GRCh37 chr5: 10,760,373-10,761,880 , GRCh38.p12 chr5: 10,760,261-10,761,768 DAP
    nsv3908449copy number variation1nstd102humanBenign GRCh37 chr18: 3,635,577-3,636,426 , GRCh38.p12 chr18: 3,635,578-3,636,427 DLGAP1
    nsv3875823copy number variation1nstd102humanBenign GRCh37 chr5: 10,761,101-10,761,769 , GRCh38.p12 chr5: 10,760,989-10,761,657 DAP
    nsv3872428copy number variation1nstd102humanBenign GRCh37 chr5: 10,761,201-10,761,769 , GRCh38.p12 chr5: 10,761,089-10,761,657 DAP
    nsv3877982copy number variation1nstd102humanBenign GRCh37 chr5: 10,761,284-10,761,769 , GRCh38.p12 chr5: 10,761,172-10,761,657 DAP
    nsv3879604copy number variation1nstd102humanBenign GRCh37 chr5: 10,702,034-10,761,829 , GRCh38.p12 chr5: 10,701,922-10,761,717 DAP
    nsv6637655copy number variation1nstd102humanUncertain significance GRCh37 chr18: 4,112,815-4,195,858 , GRCh38.p12 chr18: 4,112,815-4,195,858 DLGAP1
    nsv4457658copy number variation1nstd102humanUncertain significance GRCh37 chr18: 4,117,583-4,193,497 , GRCh38.p12 chr18: 4,117,583-4,193,497 DLGAP1
    nsv5381353copy number variation1nstd102humanUncertain significance GRCh37 chr2: 74,588,271-74,607,174 , GRCh38.p12 chr2: 74,361,144-74,380,047 DCTN1
    nsv4457670copy number variation1nstd102humanUncertain significance GRCh37 chr18: 3,743,976-3,846,248 , GRCh38.p12 chr18: 3,743,976-3,846,248 DLGAP1
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