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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125453insertion1nstd186human GRCh37 chr3: 37,141,917-37,141,925 , GRCh38.p12 chr3: 37,100,426-37,100,434 LRRFIP2
    nsv5954031insertion1nstd209human GRCh38 chr3: 37,100,378-37,100,378 , GRCh37.p13 chr3: 37,141,869-37,141,869 LRRFIP2
    nsv5687132mobile element insertion1nstd211human GRCh38 chr3: 37,074,938-37,074,938 , GRCh37.p13 chr3: 37,116,429-37,116,429 LRRFIP2
    nsv5674982mobile element insertion1nstd211human GRCh38 chr3: 37,175,250-37,175,250 , GRCh37.p13 chr3: 37,216,741-37,216,741 , LRRFIP2
    nsv5673725copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,091,967-37,092,144 , GRCh38.p12 chr3: 37,050,476-37,050,653 LRRFIP2, MLH1
    nsv5619678insertion1nstd207human GRCh38 chr3: 37,163,862-37,163,862 , GRCh37.p13 chr3: 37,205,353-37,205,353 LRRFIP2
    nsv5617096insertion1nstd207human GRCh38 chr3: 37,100,383-37,100,383 , GRCh37.p13 chr3: 37,141,874-37,141,874 LRRFIP2
    nsv5608639insertion1nstd207human GRCh38 chr3: 37,157,989-37,157,989 , GRCh37.p13 chr3: 37,199,480-37,199,480 LRRFIP2
    nsv5549824insertion1nstd206human GRCh38 chr3: 37,100,426-37,100,434 , GRCh37.p13 chr3: 37,141,917-37,141,925 LRRFIP2
    nsv5547693insertion1nstd206human GRCh38 chr3: 37,149,609-37,149,643 , GRCh37.p13 chr3: 37,191,100-37,191,134 LRRFIP2
    nsv5452818copy number variation1nstd206human GRCh38 chr3: 37,089,111-37,161,342 , GRCh37.p13 chr3: 37,130,602-37,202,833 RNU6-1301P, LRRFIP2, 2 more genes
    nsv5449666copy number variation1nstd206human GRCh38 chr3: 37,165,566-37,166,101 , GRCh37.p13 chr3: 37,207,057-37,207,592 LRRFIP2
    nsv5399512mobile element insertion1nstd206human GRCh38 chr3: 37,175,250-37,175,301 , GRCh37.p13 chr3: 37,216,741-37,216,792 , LRRFIP2
    nsv5377439translocation1nstd200human GRCh38 chr3: 37,050,719-37,050,719 , GRCh38 chr3: 37,052,037-37,052,037 , GRCh37.p13 chr3: 37,092,210-37,092,210 , GRCh37.p13 chr3: 37,093,528-37,093,528 LRRFIP2, MLH1
    nsv5351661translocation1nstd200human GRCh38 chr3: 37,131,323-37,131,323 , GRCh38 chr3: 37,147,624-37,147,624 , GRCh37.p13 chr3: 37,189,115-37,189,115 , GRCh37.p13 chr3: 37,172,814-37,172,814 LRRFIP2
    nsv5351660translocation1nstd200human GRCh38 chr3: 37,052,181-37,052,181 , GRCh38 chr3: 37,051,241-37,051,241 , GRCh37.p13 chr3: 37,092,732-37,092,732 , GRCh37.p13 chr3: 37,093,672-37,093,672 MLH1, LRRFIP2
    nsv5333837translocation1nstd200human GRCh37 chr3: 37,189,115-37,189,115 , GRCh37 chr3: 37,172,814-37,172,814 , GRCh38.p12 chr3: 37,131,323-37,131,323 , GRCh38.p12 chr3: 37,147,624-37,147,624 LRRFIP2
    nsv5315264copy number variation1nstd204human GRCh38.p13 chr3: 37,164,377-37,166,701 , GRCh37.p13 chr3: 37,205,868-37,208,192 LRRFIP2
    nsv5216545copy number variation1nstd204human GRCh38.p13 chr3: 37,161,701-37,167,600 , GRCh37.p13 chr3: 37,203,192-37,209,091 LRRFIP2
    nsv5209025copy number variation1nstd204human GRCh38.p13 chr3: 37,164,335-37,165,634 , GRCh37.p13 chr3: 37,205,826-37,207,125 LRRFIP2
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