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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112735copy number variation1nstd102humannot provided GRCh37 chr7: 6,026,390-6,027,251 , GRCh38.p12 chr7: 5,986,759-5,987,620 PMS2
    nsv5976512inversion1nstd209human GRCh38 chr7: 5,976,108-6,745,714 , GRCh37.p13 chr7: 6,015,739-6,785,345 PMS2, RAC1, 22 more genes
    nsv5847370copy number variation1nstd209human GRCh38 chr7: 6,008,721-6,009,820 , GRCh37.p13 chr7: 6,048,352-6,049,451 PMS2, AIMP2
    nsv5847369copy number variation1nstd209human GRCh38 chr7: 5,982,696-5,985,159 , GRCh37.p13 chr7: 6,022,327-6,024,790 PMS2
    nsv5674036copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,042,074-6,049,099 , GRCh38.p12 chr7: 6,002,443-6,009,468 PMS2, AIMP2
    nsv5674035copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,035,155-6,043,699 , GRCh38.p12 chr7: 5,995,524-6,004,068 PMS2
    nsv5674034copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,031,594-6,049,099 , GRCh38.p12 chr7: 5,991,963-6,009,468 PMS2, AIMP2
    nsv5674033copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,022,445-6,022,632 , GRCh38.p12 chr7: 5,982,814-5,983,001 PMS2
    nsv5673936copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,026,380-6,043,699 , GRCh38.p12 chr7: 5,986,749-6,004,068 PMS2
    nsv5673848copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,022,449-6,022,628 , GRCh38.p12 chr7: 5,982,818-5,982,997 PMS2
    nsv5667605inversion1nstd207human GRCh37.p13 chr7: 6,028,678-6,775,274 , GRCh38 chr7: 5,989,047-6,735,643 PMS2, RAC1, 22 more genes
    nsv5635987insertion1nstd207human GRCh38 chr7: 5,969,704-5,969,704 , GRCh37.p13 chr7: 6,009,335-6,009,335 PMS2, RSPH10B
    nsv5630522insertion1nstd207human GRCh38 chr7: 5,980,895-5,980,895 , GRCh37.p13 chr7: 6,020,526-6,020,526 PMS2
    nsv5564492copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 6,029,428-6,029,671 , GRCh38 chr7: 5,989,797-5,990,040 PMS2
    nsv5564491copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,017,215-6,019,662 , GRCh38 chr7: 5,977,584-5,980,031 PMS2
    nsv5564490copy number variation1nstd102humanPathogenic GRCh38 chr7: 5,973,397-5,973,982 , GRCh37 chr7: 6,013,028-6,013,613 PMS2
    nsv5564441copy number variation1nstd102humanPathogenic GRCh38 chr7: 5,991,971-5,992,256 , GRCh37 chr7: 6,031,602-6,031,887 PMS2
    nsv5564358copy number variation1nstd102humanPathogenic GRCh38 chr7: 5,989,798-5,989,956 , GRCh37 chr7: 6,029,429-6,029,587 PMS2
    nsv5564357copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,026,388-6,027,252 , GRCh38 chr7: 5,986,757-5,987,621 PMS2
    nsv5564356copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,017,217-6,017,389 , GRCh38 chr7: 5,977,586-5,977,758 PMS2
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