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Items: 1 to 20 of 195

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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
    nsv7065985inversion1nstd229human GRCh38 chr20: 63,509,212-64,282,670 , GRCh37.p13 chr20: 62,140,565-62,914,023 RNU1-134P, MIR6813, 46 more genes
    nsv7031383copy number variation1nstd229human GRCh38 chr20: 64,048,001-64,107,600 , GRCh37.p13 chr20: 62,679,354-62,738,953 OPRL1, NPBWR2, 5 more genes
    nsv7026232copy number variation1nstd229human GRCh38 chr20: 64,043,001-64,105,200 , GRCh37.p13 chr20: 62,674,354-62,736,553 LKAAEAR1, OPRL1, 5 more genes
    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
    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
    nsv6290296copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,273,854-62,907,579 , GRCh38.p12 chr20: 62,642,502-64,276,226 CHRNA4, COL9A3, 90 more genes
    nsv6284016copy number variation1nstd214human GRCh38 chr20: 64,104,465-64,104,601 , GRCh37.p13 chr20: 62,735,818-62,735,954 NPBWR2
    nsv6278553copy number variation1nstd214human GRCh38 chr20: 64,104,729-64,104,875 , GRCh37.p13 chr20: 62,736,082-62,736,228 NPBWR2
    nsv6233645insertion1nstd214human GRCh38 chr20: 64,105,770-64,105,770 , GRCh37.p13 chr20: 62,737,123-62,737,123 NPBWR2
    nsv6223840copy number variation1nstd214human GRCh38 chr20: 64,105,574-64,105,724 , GRCh37.p13 chr20: 62,736,927-62,737,077 NPBWR2
    nsv6134181copy number variation1nstd213human GRCh37 chr20: 61,440,000-62,920,001 , GRCh38.p12 chr20: 62,808,648-64,288,648 CHRNA4, KCNQ2, 82 more genes
    nsv6134180copy number variation1nstd213human GRCh37 chr20: 61,370,000-62,910,001 , GRCh38.p12 chr20: 62,738,648-64,278,648 , KCNQ2, 88 more genes
    nsv6134086copy number variation1nstd213human GRCh37 chr20: 61,270,000-62,920,001 , GRCh38.p12 chr20: 62,638,648-64,288,648 , EEF1A2, 91 more genes
    nsv6134048copy number variation1nstd213human GRCh37 chr20: 61,440,000-62,930,001 , GRCh38.p12 chr20: 62,808,648-64,298,648 CHRNA4, KCNQ2, 84 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
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