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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096716copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,034,542-37,042,554 , GRCh38.p12 chr3: 36,993,051-37,001,063 MLH1, EPM2AIP1
    nsv7096715copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,034,542-37,035,260 , GRCh38.p12 chr3: 36,993,051-36,993,769 EPM2AIP1, MLH1
    nsv7096564copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,034,542-37,061,964 , GRCh38.p12 chr3: 36,993,051-37,020,473 EPM2AIP1, RPL29P11, 1 more genes
    nsv7096463copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,034,870-37,035,863 , GRCh38.p12 chr3: 36,993,379-36,994,372 EPM2AIP1, MLH1
    nsv7045019inversion1nstd229human GRCh38 chr3: 36,791,735-37,434,975 , GRCh37.p13 chr3: 36,833,226-37,476,466 GOLGA4-AS1, RPS16P4, 17 more genes
    nsv7044784inversion1nstd229human GRCh38 chr3: 36,978,242-36,985,408 , GRCh37.p13 chr3: 37,019,733-37,026,899 EPM2AIP1
    nsv6709671copy number variation1nstd229human GRCh38 chr3: 33,814,589-38,161,211 , GRCh37.p13 chr3: 33,856,081-38,202,702 RFC3P1, ITGA9, 51 more genes
    nsv6702826copy number variation1nstd229human GRCh38 chr3: 36,968,490-36,984,532 , GRCh37.p13 chr3: 37,009,981-37,026,023 PRADC1P1, EPM2AIP1, 1 more genes
    nsv6636559copy number variation1nstd102humanUncertain significance GRCh37 chr3: 36,948,417-37,028,790 , GRCh38.p12 chr3: 36,906,926-36,987,299 PRADC1P1, EPM2AIP1, 2 more genes
    nsv6548825inversion1nstd223human GRCh38 chr3: 36,984,006-36,984,858 , GRCh37.p13 chr3: 37,025,497-37,026,349 EPM2AIP1
    nsv6357813copy number variation1nstd223human GRCh38 chr3: 36,978,156-36,985,404 , GRCh37.p13 chr3: 37,019,647-37,026,895 EPM2AIP1
    nsv6311982copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,034,542-38,835,501 , GRCh38.p12 chr3: 36,993,051-38,794,010 SCN10A, PPP2R2DP1, 41 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6311791copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,034,542-37,059,100 , GRCh38.p12 chr3: 36,993,051-37,017,609 MLH1, RPL29P11, 1 more genes
    nsv6311454copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,034,816-37,037,072 , GRCh38.p12 chr3: 36,993,325-36,995,581 MLH1, EPM2AIP1
    nsv5673561copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,035,033-37,035,160 , GRCh38.p12 chr3: 36,993,542-36,993,669 MLH1, EPM2AIP1
    nsv5673467copy number variation1nstd102humanPathogenic GRCh38 chr3: 36,993,164-36,997,312 , GRCh37 chr3: 37,034,655-37,038,803 MLH1, EPM2AIP1
    nsv5564255copy number variation1nstd102humanPathogenic GRCh38 chr3: 36,993,546-36,993,664 , GRCh37 chr3: 37,035,037-37,035,155 EPM2AIP1, MLH1
    nsv5562379sequence alteration1nstd206human GRCh38 chr3: 36,978,157-36,985,404 , GRCh37.p13 chr3: 37,019,648-37,026,895 EPM2AIP1
    nsv5443040copy number variation1nstd206human GRCh38 chr3: 36,990,452-36,990,508 , GRCh37.p13 chr3: 37,031,943-37,031,999 EPM2AIP1
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