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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128289copy number variation1nstd186human GRCh37 chr22: 41,870,367-41,870,673 , GRCh38.p12 chr22: 41,474,363-41,474,669 ACO2
    nsv5962194copy number variation1nstd209human GRCh38 chr22: 41,485,461-41,486,503 , GRCh37.p13 chr22: 41,881,465-41,882,507 ACO2
    nsv5872951copy number variation1nstd209human GRCh38 chr22: 41,485,406-41,487,919 , GRCh37.p13 chr22: 41,881,410-41,883,923 ACO2
    nsv5715192mobile element insertion1nstd211human GRCh38 chr22: 41,513,347-41,513,347 , GRCh37.p13 chr22: 41,909,351-41,909,351 ACO2
    nsv5547604copy number variation1nstd206human GRCh38 chr22: 41,500,022-41,548,873 , GRCh37.p13 chr22: 41,896,026-41,944,877 POLR3H, ACO2
    nsv5544445copy number variation1nstd206human GRCh38 chr22: 41,474,343-41,474,689 , GRCh37.p13 chr22: 41,870,347-41,870,693 ACO2
    nsv5541501copy number variation1nstd206human GRCh38 chr22: 41,485,435-41,486,461 , GRCh37.p13 chr22: 41,881,439-41,882,465 ACO2
    nsv5537560copy number variation1nstd206human GRCh38 chr22: 41,495,889-41,502,862 , GRCh37.p13 chr22: 41,891,893-41,898,866 ACO2
    nsv5537250copy number variation1nstd206human GRCh38 chr22: 41,502,754-41,503,410 , GRCh37.p13 chr22: 41,898,758-41,899,414 ACO2
    nsv5381158copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,918,834-41,923,424 , GRCh38.p12 chr22: 41,522,830-41,527,420 ACO2, POLR3H
    nsv5299062copy number variation1nstd204human GRCh38.p13 chr22: 41,442,501-41,665,900 , GRCh37.p13 chr22: 41,838,505-42,061,904 CSDC2, LOC105373043, 8 more genes
    nsv5293624copy number variation1nstd204human GRCh38.p13 chr22: 41,236,101-41,543,100 , GRCh37.p13 chr22: 41,632,105-41,939,104 LOC105373042, RANGAP1, 11 more genes
    nsv5286543copy number variation1nstd204human GRCh38.p13 chr22: 41,468,768-41,471,367 , GRCh37.p13 chr22: 41,864,772-41,867,371 PHF5A, ACO2
    nsv5281292copy number variation1nstd204human GRCh38.p13 chr22: 41,124,301-41,900,100 , GRCh37.p13 chr22: 41,520,305-42,296,104 SNU13, RANGAP1, 34 more genes
    nsv5215468mobile element deletion1nstd204human GRCh38.p13 chr22: 41,485,411-41,485,771 , GRCh37.p13 chr22: 41,881,415-41,881,775 ACO2
    nsv5196146mobile element insertion1nstd203human GRCh38 chr22: 41,513,333-41,513,347 , GRCh37.p13 chr22: 41,909,337-41,909,351 ACO2
    nsv5191686mobile element insertion1nstd203human GRCh38 chr22: 41,513,337-41,513,347 , GRCh37.p13 chr22: 41,909,341-41,909,351 ACO2
    nsv5040661copy number variation1nstd200human GRCh38 chr22: 41,503,966-41,504,087 , GRCh37.p13 chr22: 41,899,970-41,900,091 ACO2
    nsv5036675copy number variation1nstd200human GRCh38 chr22: 41,477,411-41,485,621 , GRCh37.p13 chr22: 41,873,415-41,881,625 ACO2
    nsv5032425inversion1nstd200human GRCh38 chr22: 41,452,969-44,153,937 , GRCh37.p13 chr22: 41,848,973-44,549,817 , LOC101927393, 95 more genes
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