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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953178insertion1nstd209human GRCh38 chr6: 18,396,321-18,396,321 , GRCh37.p13 chr6: 18,396,552-18,396,552 RNF144B
    nsv5903147copy number variation1nstd209human GRCh38 chr6: 18,451,502-18,451,648 , GRCh37.p13 chr6: 18,451,733-18,451,879 RNF144B
    nsv5891207copy number variation1nstd209human GRCh38 chr6: 18,401,856-18,402,635 , GRCh37.p13 chr6: 18,402,087-18,402,866 RNF144B
    nsv5722449mobile element insertion1nstd211human GRCh38 chr6: 18,466,631-18,466,631 , GRCh37.p13 chr6: 18,466,862-18,466,862 RNF144B
    nsv5688061mobile element insertion1nstd211human GRCh38 chr6: 18,454,991-18,454,991 , GRCh37.p13 chr6: 18,455,222-18,455,222 RNF144B
    nsv5567861copy number variation1nstd207human GRCh38 chr6: 18,401,856-18,402,635 , GRCh37.p13 chr6: 18,402,087-18,402,866 RNF144B
    nsv5456481copy number variation1nstd206human GRCh38 chr6: 18,401,859-18,402,636 , GRCh37.p13 chr6: 18,402,090-18,402,867 RNF144B
    nsv5314363copy number variation1nstd204human GRCh38.p13 chr6: 18,401,859-18,402,636 , GRCh37.p13 chr6: 18,402,090-18,402,867 RNF144B
    nsv5224612copy number variation1nstd204human GRCh38.p13 chr6: 18,401,901-18,402,600 , GRCh37.p13 chr6: 18,402,132-18,402,831 RNF144B
    nsv5088857mobile element insertion1nstd203human GRCh38 chr6: 18,423,928-18,423,939 , GRCh37.p13 chr6: 18,424,159-18,424,170 RNF144B
    nsv5081595mobile element insertion1nstd203human GRCh38 chr6: 18,430,672-18,430,722 , GRCh37.p13 chr6: 18,430,903-18,430,953 RNF144B
    nsv4932976copy number variation1nstd200human GRCh38 chr6: 18,401,859-18,402,636 , GRCh37.p13 chr6: 18,402,090-18,402,867 RNF144B
    nsv4809915copy number variation1nstd200human GRCh37 chr6: 18,402,090-18,402,867 , GRCh38.p12 chr6: 18,401,859-18,402,636 RNF144B
    nsv4809913copy number variation1nstd200human GRCh37 chr6: 18,375,418-18,521,300 , GRCh38.p12 chr6: 18,375,187-18,521,069 MIR548A1HG, RNF144B, 1 more genes
    nsv4749862copy number variation1nstd199human GRCh37 chr6: 18,402,084-18,402,865 , GRCh38.p12 chr6: 18,401,853-18,402,634 RNF144B
    nsv4705556copy number variation3nstd195human GRCh37 chr6: 18,402,087-18,402,088 , GRCh38.p12 chr6: 18,401,856-18,401,857 RNF144B
    nsv4663587copy number variation1nstd186human GRCh37 chr6: 18,402,120-18,402,881 , GRCh38.p12 chr6: 18,401,889-18,402,650 RNF144B
    nsv4654462copy number variation1nstd186human GRCh37 chr6: 18,402,131-18,402,447 , GRCh38.p12 chr6: 18,401,900-18,402,216 RNF144B
    nsv4640955copy number variation1nstd186human GRCh37 chr6: 18,402,112-18,402,924 , GRCh38.p12 chr6: 18,401,881-18,402,693 RNF144B
    nsv4638186copy number variation3nstd186human GRCh37 chr6: 18,402,090-18,402,867 , GRCh38.p12 chr6: 18,401,859-18,402,636 RNF144B
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