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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129555insertion1nstd186human GRCh37 chr20: 58,889,661-58,889,723 , GRCh38.p12 chr20: 60,314,603-60,314,665 MIR646HG
    nsv6127915copy number variation1nstd186human GRCh37 chr20: 58,889,425-58,889,831 , GRCh38.p12 chr20: 60,314,367-60,314,773 MIR646HG
    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
    nsv5976798insertion1nstd209human GRCh38 chr20: 60,180,611-60,180,611 , GRCh37.p13 chr20: 58,755,669-58,755,669 MIR646HG
    nsv5966731copy number variation1nstd209human GRCh38 chr20: 60,307,142-60,307,267 , GRCh37.p13 chr20: 58,882,200-58,882,325 MIR646, MIR646HG
    nsv5960922copy number variation1nstd209human GRCh38 chr20: 60,277,507-60,277,580 , GRCh37.p13 chr20: 58,852,565-58,852,638 MIR646HG, LOC105372698
    nsv5710724mobile element insertion2nstd211human GRCh38 chr20: 60,180,621-60,180,621 , GRCh37.p13 chr20: 58,755,679-58,755,679 MIR646HG
    nsv5706459mobile element insertion1nstd211human GRCh38 chr20: 60,207,970-60,207,970 , GRCh37.p13 chr20: 58,783,028-58,783,028 MIR646HG
    nsv5695631mobile element insertion2nstd211human GRCh38 chr20: 60,201,210-60,201,210 , GRCh37.p13 chr20: 58,776,268-58,776,268 MIR646HG
    nsv5672376insertion1nstd207human GRCh38 chr20: 60,314,587-60,314,587 , GRCh37.p13 chr20: 58,889,645-58,889,645 MIR646HG
    nsv5669794insertion1nstd207human GRCh38 chr20: 60,299,572-60,299,572 , GRCh37.p13 chr20: 58,874,630-58,874,630 MIR646HG
    nsv5669738insertion1nstd207human GRCh38 chr20: 60,314,711-60,314,711 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN MIR646HG
    nsv5669106insertion1nstd207human GRCh38 chr20: 60,314,444-60,314,444 , GRCh37.p13 chr20: 58,889,502-58,889,502 MIR646HG
    nsv5603421copy number variation1nstd207human GRCh38 chr20: 60,307,142-60,307,267 , GRCh37.p13 chr20: 58,882,200-58,882,325 MIR646, MIR646HG
    nsv5544032insertion1nstd206human GRCh38 chr20: 60,314,603-60,314,665 , GRCh37.p13 chr20: 58,889,661-58,889,723 MIR646HG
    nsv5533487copy number variation1nstd206human GRCh38 chr20: 60,180,405-60,197,562 , GRCh37.p13 chr20: 58,755,463-58,772,620 MIR646HG
    nsv5532776copy number variation1nstd206human GRCh38 chr20: 60,314,367-60,314,773 , GRCh37.p13 chr20: 58,889,425-58,889,831 MIR646HG
    nsv5529756copy number variation1nstd206human GRCh38 chr20: 60,133,731-60,146,471 , GRCh37.p13 chr20: 58,708,787-58,721,527 MIR646HG
    nsv5526934copy number variation1nstd206human GRCh38 chr20: 60,169,677-60,170,896 , GRCh37.p13 chr20: 58,744,735-58,745,954 MIR646HG
    nsv5525967copy number variation1nstd206human GRCh38 chr20: 60,307,142-60,307,268 , GRCh37.p13 chr20: 58,882,200-58,882,326 MIR646, MIR646HG
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