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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885006copy number variation1nstd209human GRCh38 chr1: 168,055,321-168,056,493 , GRCh37.p13 chr1: 168,024,559-168,025,731 DCAF6, GCSHP5
    nsv5882956copy number variation1nstd209human GRCh38 chr1: 167,980,339-167,980,419 , GRCh37.p13 chr1: 167,949,577-167,949,657 DCAF6
    nsv5877186copy number variation1nstd209human GRCh38 chr1: 168,073,952-168,074,064 , GRCh37.p13 chr1: 168,043,190-168,043,302 DCAF6
    nsv5582517copy number variation1nstd207human GRCh38 chr1: 168,055,321-168,056,493 , GRCh37.p13 chr1: 168,024,559-168,025,731 GCSHP5, DCAF6
    nsv5534491insertion1nstd206human GRCh38 chr1: 168,040,341-168,040,343 , GRCh37.p13 chr1: 168,009,579-168,009,581 DCAF6
    nsv5426078copy number variation1nstd206human GRCh38 chr1: 167,980,339-167,980,422 , GRCh37.p13 chr1: 167,949,577-167,949,660 DCAF6
    nsv5425925copy number variation1nstd206human GRCh38 chr1: 168,055,316-168,056,514 , GRCh37.p13 chr1: 168,024,554-168,025,752 DCAF6, GCSHP5
    nsv5422246copy number variation1nstd206human GRCh38 chr1: 167,997,437-167,997,551 , GRCh37.p13 chr1: 167,966,675-167,966,789 MIR1255B2, DCAF6
    nsv5382843copy number variation2nstd186human GRCh37 chr1: 168,024,574-168,025,732 , GRCh38.p12 chr1: 168,055,336-168,056,494 DCAF6, GCSHP5
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5379140translocation1nstd200human GRCh38 chr19: 23,850,376-23,850,376 , GRCh38 chr1: 168,056,494-168,056,494 , GRCh37.p13 chr1: 168,025,732-168,025,732 , GRCh37.p13 chr19: 24,033,178-24,033,178 GCSHP5, DCAF6
    nsv5379134translocation1nstd200human GRCh38 chr1: 168,055,346-168,055,346 , GRCh38 chr19: 23,850,382-23,850,382 , GRCh37.p13 chr1: 168,024,584-168,024,584 , GRCh37.p13 chr19: 24,033,184-24,033,184 DCAF6, GCSHP5
    nsv5334040translocation1nstd200human GRCh37 chr1: 168,024,584-168,024,584 , GRCh37 chr19: 24,033,184-24,033,184 , GRCh38.p12 chr1: 168,055,346-168,055,346 , GRCh38.p12 chr19: 23,850,382-23,850,382 GCSHP5, DCAF6
    nsv5325930translocation1nstd204human GRCh37.p13 chr1: 168,024,584-168,024,584 , GRCh37.p13 chr19: 24,033,184-24,033,184 , GRCh38.p13 chr1: 168,055,346-168,055,346 , GRCh38.p13 chr19: 23,850,382-23,850,382 DCAF6, GCSHP5
    nsv5297224copy number variation1nstd204human GRCh37.p13 chr1: 168,024,574-168,025,732 , GRCh38.p13 chr1: 168,055,336-168,056,494 GCSHP5, DCAF6
    nsv5281252copy number variation1nstd204human GRCh37.p13 chr1: 167,967,822-167,970,205 , GRCh38.p13 chr1: 167,998,584-168,000,967 DCAF6, MIR1255B2
    nsv5218795copy number variation1nstd204human GRCh38.p13 chr1: 167,998,601-168,001,000 , GRCh37.p13 chr1: 167,967,839-167,970,238 MIR1255B2, DCAF6
    nsv5209352copy number variation1nstd204human GRCh38.p13 chr1: 167,998,626-168,001,000 , GRCh37.p13 chr1: 167,967,864-167,970,238 DCAF6, MIR1255B2
    nsv5204242copy number variation1nstd204human GRCh38.p13 chr1: 168,055,301-168,056,500 , GRCh37.p13 chr1: 168,024,539-168,025,738 DCAF6, GCSHP5
    nsv5191426mobile element insertion1nstd203human GRCh38 chr1: 168,021,158-168,021,171 , GRCh37.p13 chr1: 167,990,396-167,990,409 DCAF6
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