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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682973copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,011,870-6,049,737 , GRCh38.p12 chr7: 5,972,239-6,010,106 AIMP2, PMS2
    nsv4682649copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,026,380-6,048,747 , GRCh38.p12 chr7: 5,986,749-6,009,116 AIMP2, PMS2
    nsv1398169copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,029,431-6,048,737 , GRCh38 chr7: 5,989,800-6,009,106 AIMP2, PMS2
    nsv4681563copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,029,421-6,048,660 , GRCh38.p12 chr7: 5,989,790-6,009,029 AIMP2, PMS2
    nsv3886927copy number variation1nstd102humanPathogenic GRCh38 chr7: 5,991,973-6,009,106 , GRCh37 chr7: 6,031,604-6,048,737 AIMP2, PMS2
    nsv3870947copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,031,594-6,048,660 , GRCh38 chr7: 5,991,963-6,009,029 AIMP2, PMS2
    nsv6312455copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,035,155-6,049,099 , GRCh38.p12 chr7: 5,995,524-6,009,468 AIMP2, PMS2
    nsv6312784copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,038,729-6,049,099 , GRCh38.p12 chr7: 5,999,098-6,009,468 AIMP2, PMS2
    nsv3872006copy number variation1nstd102humanPathogenic GRCh38 chr7: 5,999,102-6,009,025 , GRCh37 chr7: 6,038,733-6,048,656 AIMP2, PMS2
    nsv6312866copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,043,311-6,049,099 , GRCh38.p12 chr7: 6,003,680-6,009,468 AIMP2, PMS2
    nsv6312785copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,045,513-6,049,099 , GRCh38.p12 chr7: 6,005,882-6,009,468 AIMP2, PMS2
    nsv4681768copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,048,556-6,049,099 , GRCh38.p12 chr7: 6,008,925-6,009,468 AIMP2, PMS2
    nsv1398050copy number variation1nstd102humanPathogenic GRCh37 chr7: 6,048,628-6,048,737 , GRCh38 chr7: 6,008,997-6,009,106 AIMP2, PMS2
    nsv3879628copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,026,380-6,048,660 , GRCh38 chr7: 5,986,749-6,009,029 AIMP2, PMS2
    nsv3888333copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,026,384-6,048,656 , GRCh38 chr7: 5,986,753-6,009,025 AIMP2, PMS2
    nsv5674034copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,031,594-6,049,099 , GRCh38.p12 chr7: 5,991,963-6,009,468 AIMP2, PMS2
    nsv5674036copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 6,042,074-6,049,099 , GRCh38.p12 chr7: 6,002,443-6,009,468 AIMP2, PMS2
    nsv1398383copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,026,390-6,048,651 , GRCh38 chr7: 5,986,759-6,009,020 AIMP2, PMS2
    nsv3888798copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,042,078-6,048,656 , GRCh38 chr7: 6,002,447-6,009,025 AIMP2, PMS2
    nsv7098129copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,048,618-6,049,099 , GRCh38.p12 chr7: 6,008,987-6,009,468 AIMP2, PMS2
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