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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634496copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,614,482-23,652,679 , GRCh38.p12 chr16: 23,603,161-23,641,358 DCTN5, PALB2
    nsv4683658copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,614,770-23,652,488 , GRCh38.p12 chr16: 23,603,449-23,641,167 DCTN5, PALB2
    nsv4681963copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,625,413-23,652,678 , GRCh38.p12 chr16: 23,614,092-23,641,357 DCTN5, PALB2
    nsv7094573copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,625,315-23,652,478 , GRCh38.p12 chr16: 23,613,994-23,641,157 DCTN5, PALB2
    nsv3879287copy number variation1nstd102humanPathogenic GRCh38 chr16: 23,621,362-23,641,357 , GRCh37.p13 chr16: 23,632,683-23,652,678 DCTN5, PALB2
    nsv3872860copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,632,673-23,652,488 , GRCh38 chr16: 23,621,352-23,641,167 DCTN5, PALB2
    nsv6310070copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,635,320-23,652,478 , GRCh38.p12 chr16: 23,623,999-23,641,157 DCTN5, PALB2
    nsv4681233copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,637,719-23,652,430 , GRCh38.p12 chr16: 23,626,398-23,641,109 DCTN5, PALB2
    nsv4681615copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,640,515-23,652,478 , GRCh38.p12 chr16: 23,629,194-23,641,157 DCTN5, PALB2
    nsv4454788copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,646,173-23,652,488 , GRCh38 chr16: 23,634,852-23,641,167 DCTN5, PALB2
    nsv3881908copy number variation1nstd102humanPathogenic GRCh38 chr16: 23,634,856-23,641,163 , GRCh37 chr16: 23,646,177-23,652,484 DCTN5, PALB2
    nsv4452815copy number variation1nstd102humanPathogenic GRCh38 chr16: 23,637,840-23,641,167 , GRCh37 chr16: 23,649,161-23,652,488 DCTN5, PALB2
    nsv6309861copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,652,421-23,652,478 , GRCh38.p12 chr16: 23,641,100-23,641,157 DCTN5, PALB2
    nsv3886204copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 23,614,483-23,652,678 , GRCh38 chr16: 23,603,162-23,641,357 DCTN5, PALB2
    nsv4682362copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr16: 23,614,634-23,652,478 , GRCh38.p12 chr16: 23,603,313-23,641,157 DCTN5, PALB2
    nsv5672923copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr16: 23,619,175-23,652,478 , GRCh38.p12 chr16: 23,607,854-23,641,157 DCTN5, PALB2
    nsv6634527copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 23,652,313-23,652,470 , GRCh38 chr16: 23,640,992-23,641,149 DCTN5, PALB2
    nsv4452117copy number variation1nstd102humanUncertain significance GRCh38 chr16: 23,603,449-23,641,167 , GRCh37 chr16: 23,614,770-23,652,488 DCTN5, PALB2
    nsv4683113copy number variation1nstd102humanUncertain significance GRCh37 chr16: 23,640,515-23,652,488 , GRCh38.p12 chr16: 23,629,194-23,641,167 DCTN5, PALB2
    nsv3870666copy number variation1nstd102humanUncertain significance GRCh37 chr16: 23,646,183-23,652,678 , GRCh38 chr16: 23,634,862-23,641,357 DCTN5, PALB2
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