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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7096087copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,559,699-62,680,869 , GRCh38.p12 chr20: 63,928,346-64,049,516 ZNF512B, MIR647, 9 more genes
    nsv7065985inversion1nstd229human GRCh38 chr20: 63,509,212-64,282,670 , GRCh37.p13 chr20: 62,140,565-62,914,023 RNU1-134P, MIR6813, 46 more genes
    nsv7061289inversion1nstd229human GRCh38 chr20: 63,026,492-64,008,482 , GRCh37.p13 chr20: 61,657,844-62,639,835 TNFRSF6B, MIR941-5, 60 more genes
    nsv7059476inversion1nstd229human GRCh38 chr20: 63,024,183-64,005,567 , GRCh37.p13 chr20: 61,655,535-62,636,920 RTEL1-TNFRSF6B, LOC105372721, 60 more genes
    nsv7029144copy number variation1nstd229human GRCh38 chr20: 63,975,310-63,975,371 , GRCh37.p13 chr20: 62,606,663-62,606,724 SAMD10
    nsv7028684copy number variation1nstd229human GRCh38 chr20: 63,981,082-63,981,441 , GRCh37.p13 chr20: 62,612,435-62,612,794 SAMD10, PRPF6
    nsv7027026copy number variation1nstd229human GRCh38 chr20: 63,882,924-63,972,300 , GRCh37.p13 chr20: 62,514,277-62,603,653 MIR941-1, MIR941-3, 12 more genes
    nsv7026005copy number variation1nstd229human GRCh38 chr20: 63,976,112-63,987,414 , GRCh37.p13 chr20: 62,607,465-62,618,767 SAMD10, PRPF6
    nsv7023017copy number variation1nstd229human GRCh38 chr20: 63,963,337-63,974,429 , GRCh37.p13 chr20: 62,594,690-62,605,782 ZNF512B, SAMD10
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6626834copy number variation1nstd224human GRCh37 chr20: 62,586,262-62,608,325 , GRCh38.p12 chr20: 63,954,909-63,976,972 UCKL1-AS1, UCKL1, 2 more genes
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 HAR1A, PPDPF, 100 more genes
    nsv6314091copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202 TPD52L2, MIR941-5, 72 more genes
    nsv6291738copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202 PTK6, C20orf204, 63 more genes
    nsv6290337copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,038,552-62,907,579 , GRCh38.p12 chr20: 62,463,496-64,276,226 CHRNA4, COL9A3, 99 more genes
    nsv6290321copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,826,780-62,660,844 , GRCh38.p12 chr20: 63,195,428-64,029,491 CHRNA4, EEF1A2, 51 more genes
    nsv6290297copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,041,481-62,680,992 , GRCh38.p12 chr20: 62,466,425-64,049,639 CHRNA4, COL9A3, 91 more genes
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