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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129729insertion1nstd186human GRCh37 chr20: 61,982,535-61,982,538 , GRCh38.p12 chr20: 63,351,183-63,351,186 CHRNA4
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5976999insertion1nstd209human GRCh38 chr20: 63,361,431-63,361,431 , GRCh37.p13 chr20: 61,992,783-61,992,783 LOC100130587, CHRNA4
    nsv5971626insertion1nstd209human GRCh38 chr20: 63,351,184-63,351,184 , GRCh37.p13 chr20: 61,982,536-61,982,536 CHRNA4
    nsv5971110insertion1nstd209human GRCh38 chr20: 63,353,915-63,353,915 , GRCh37.p13 chr20: 61,985,267-61,985,267 CHRNA4
    nsv5953510copy number variation1nstd209human GRCh38 chr20: 63,354,216-63,354,473 , GRCh37.p13 chr20: 61,985,568-61,985,825 CHRNA4
    nsv5673419copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,977,556-62,078,210 , GRCh38.p12 chr20: 63,346,204-63,446,857 CHRNA4, KCNQ2, 4 more genes
    nsv5673179copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,977,556-62,039,909 , GRCh38.p12 chr20: 63,346,204-63,408,556 LOC100130587, KCNQ2, 1 more genes
    nsv5672334insertion1nstd207human GRCh38 chr20: 63,351,183-63,351,183 , GRCh37.p13 chr20: 61,982,535-61,982,535 CHRNA4
    nsv5671031insertion1nstd207human GRCh38 chr20: 63,354,271-63,354,271 , GRCh37.p13 chr20: 61,985,623-61,985,623 CHRNA4
    nsv5670176insertion2nstd207human GRCh38 chr20: 63,361,431-63,361,431 , GRCh37.p13 chr20: 61,992,783-61,992,783 LOC100130587, CHRNA4
    nsv5670128insertion1nstd207human GRCh38 chr20: 63,353,917-63,353,917 , GRCh37.p13 chr20: 61,985,269-61,985,269 CHRNA4
    nsv5669342insertion1nstd207human GRCh38 chr20: 63,366,229-63,366,229 , GRCh37.p13 chr20: 61,997,581-61,997,581 CHRNA4, LOC100130587
    nsv5669274insertion1nstd207human GRCh38 chr20: 63,354,095-63,354,095 , GRCh37.p13 chr20: 61,985,447-61,985,447 CHRNA4
    nsv5666739insertion1nstd207human GRCh38 chr20: 63,354,474-63,354,474 , GRCh37.p13 chr20: 61,985,826-61,985,826 CHRNA4
    nsv5601045copy number variation1nstd207human GRCh38 chr20: 63,357,137-63,357,214 , GRCh37.p13 chr20: 61,988,489-61,988,566 CHRNA4
    nsv5595936copy number variation1nstd207human GRCh38 chr20: 63,353,936-63,354,226 , GRCh37.p13 chr20: 61,985,288-61,985,578 CHRNA4
    nsv5591539copy number variation1nstd207human GRCh38 chr20: 63,366,131-63,366,210 , GRCh37.p13 chr20: 61,997,483-61,997,562 CHRNA4, LOC100130587
    nsv5586615copy number variation1nstd207human GRCh38 chr20: 63,372,252-63,372,399 , GRCh37.p13 chr20: 62,003,604-62,003,751 CHRNA4
    nsv5586407copy number variation1nstd207human GRCh38 chr20: 63,372,178-63,372,251 , GRCh37.p13 chr20: 62,003,530-62,003,603 CHRNA4
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