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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7095204copy number variation1nstd102humanPathogenic GRCh37 chr19: 39,074,134-39,077,236 , GRCh38.p12 chr19: 38,583,494-38,586,596 MAP4K1, RYR1
    nsv7017337copy number variation1nstd229human GRCh38 chr19: 38,396,742-38,612,341 , GRCh37.p13 chr19: 38,887,382-39,102,981 SPRED3, MAP4K1, 4 more genes
    nsv7011445copy number variation1nstd229human GRCh38 chr19: 38,591,544-38,592,916 , GRCh37.p13 chr19: 39,082,184-39,083,556 MAP4K1
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6999492copy number variation1nstd229human GRCh38 chr19: 38,591,184-38,592,874 , GRCh37.p13 chr19: 39,081,824-39,083,514 MAP4K1
    nsv6517584copy number variation1nstd223human GRCh38 chr19: 38,602,301-38,603,500 , GRCh37.p13 chr19: 39,092,941-39,094,140 MAP4K1
    nsv6516944copy number variation1nstd223human GRCh38 chr19: 38,591,184-38,592,874 , GRCh37.p13 chr19: 39,081,824-39,083,514 MAP4K1
    nsv6516258copy number variation1nstd223human GRCh38 chr19: 38,602,650-38,603,102 , GRCh37.p13 chr19: 39,093,290-39,093,742 MAP4K1
    nsv6310530copy number variation1nstd102humanPathogenic GRCh37 chr19: 39,075,563-39,078,060 , GRCh38.p12 chr19: 38,584,923-38,587,420 RYR1, MAP4K1
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6286699insertion1nstd214human GRCh38 chr19: 38,602,567-38,602,567 , GRCh37.p13 chr19: 39,093,207-39,093,207 MAP4K1
    nsv6285623insertion1nstd214human GRCh38 chr19: 38,602,508-38,602,508 , GRCh37.p13 chr19: 39,093,148-39,093,148 MAP4K1
    nsv6226582copy number variation1nstd214human GRCh38 chr19: 38,603,072-38,603,129 , GRCh37.p13 chr19: 39,093,712-39,093,769 MAP4K1
    nsv6221920copy number variation1nstd214human GRCh38 chr19: 38,602,732-38,602,803 , GRCh37.p13 chr19: 39,093,372-39,093,443 MAP4K1
    nsv6213267copy number variation1nstd214human GRCh38 chr19: 38,602,957-38,603,022 , GRCh37.p13 chr19: 39,093,597-39,093,662 MAP4K1
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6111789insertion1nstd212human GRCh38 chr19: 38,603,361-38,603,361 , GRCh37.p13 chr19: 39,094,001-39,094,001 MAP4K1
    nsv6103686insertion1nstd212human GRCh38 chr19: 38,590,269-38,590,269 , GRCh37.p13 chr19: 39,080,909-39,080,909 MAP4K1
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