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Items: 1 to 20 of 367

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096798copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,061,789-37,083,832 , GRCh38.p12 chr3: 37,020,298-37,042,341 MLH1
    nsv7096717copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 37,050,291-37,061,964 , GRCh38.p12 chr3: 37,008,800-37,020,473 MLH1, RPL29P11
    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
    nsv7096565copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,037,900-37,038,207 , GRCh38.p12 chr3: 36,996,409-36,996,716 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
    nsv7096464copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,061,789-37,061,964 , GRCh38.p12 chr3: 37,020,298-37,020,473 MLH1
    nsv7096463copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,034,870-37,035,863 , GRCh38.p12 chr3: 36,993,379-36,994,372 EPM2AIP1, MLH1
    nsv7093412delins1nstd102humanLikely pathogenic GRCh37 chr3: 37,048,516-37,049,074 , GRCh38 chr3: 37,007,025-37,007,583 MLH1
    nsv7051268inversion1nstd229human GRCh38 chr3: 37,000,362-39,352,689 , GRCh37.p13 chr3: 37,041,853-39,394,180 PLCD1, RNU6-1227P, 59 more genes
    nsv7045019inversion1nstd229human GRCh38 chr3: 36,791,735-37,434,975 , GRCh37.p13 chr3: 36,833,226-37,476,466 GOLGA4-AS1, RPS16P4, 17 more genes
    nsv6714741copy number variation1nstd229human GRCh38 chr3: 37,047,962-37,059,589 , GRCh37.p13 chr3: 37,089,453-37,101,080 LRRFIP2, MLH1
    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
    nsv6706622copy number variation1nstd229human GRCh38 chr3: 37,035,271-37,035,820 , GRCh37.p13 chr3: 37,076,762-37,077,311 MLH1
    nsv6704671copy number variation1nstd229human GRCh38 chr3: 37,041,455-37,045,087 , GRCh37.p13 chr3: 37,082,946-37,086,578 MLH1
    nsv6702272copy number variation1nstd229human GRCh38 chr3: 37,032,802-37,035,339 , GRCh37.p13 chr3: 37,074,293-37,076,830 MLH1
    nsv6700113copy number variation1nstd229human GRCh38 chr3: 37,045,688-37,052,538 , GRCh37.p13 chr3: 37,087,179-37,094,029 LRRFIP2, MLH1
    nsv6634708delins1nstd102humanLikely pathogenic GRCh37 chr3: 37,061,776-37,061,930 , GRCh38 chr3: 37,020,285-37,020,439 MLH1
    nsv6634705delins1nstd102humanLikely pathogenic GRCh37 chr3: 37,056,015-37,056,117 , GRCh38 chr3: 37,014,524-37,014,626 MLH1, RPL29P11
    nsv6634698delins1nstd102humanPathogenic GRCh37 chr3: 37,090,048-37,090,048 , GRCh38 chr3: 37,048,557-37,048,557 MLH1
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