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Items: 1 to 20 of 377

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098336copy number variation1nstd102humanUncertain significance GRCh37 chrX: 84,600,846-85,302,644 , GRCh38.p12 chrX: 85,345,840-86,047,640 CHM, SFR1P2, 3 more genes
    nsv7090057copy number variation1nstd229human GRCh38 chrX: 85,380,012-85,380,055 , GRCh37.p13 chrX: 84,635,017-84,635,060 POF1B
    nsv7090056copy number variation1nstd229human GRCh38 chrX: 85,368,102-85,368,195 , GRCh37.p13 chrX: 84,623,107-84,623,200 POF1B
    nsv7090055copy number variation1nstd229human GRCh38 chrX: 85,360,801-85,363,300 , GRCh37.p13 chrX: 84,615,806-84,618,305 POF1B
    nsv7090054copy number variation1nstd229human GRCh38 chrX: 85,360,501-85,366,000 , GRCh37.p13 chrX: 84,615,506-84,621,005 POF1B
    nsv7090053copy number variation1nstd229human GRCh38 chrX: 85,337,482-85,337,661 , GRCh37.p13 chrX: 84,592,488-84,592,667 POF1B
    nsv7090052copy number variation1nstd229human GRCh38 chrX: 85,314,101-85,316,800 , GRCh37.p13 chrX: 84,569,107-84,571,806 POF1B
    nsv7090051copy number variation1nstd229human GRCh38 chrX: 85,311,701-85,314,100 , GRCh37.p13 chrX: 84,566,707-84,569,106 POF1B
    nsv7090050copy number variation1nstd229human GRCh38 chrX: 85,311,301-85,313,900 , GRCh37.p13 chrX: 84,566,307-84,568,906 POF1B
    nsv7090049copy number variation1nstd229human GRCh38 chrX: 85,285,860-85,285,924 , GRCh37.p13 chrX: 84,540,866-84,540,930 POF1B
    nsv7090048copy number variation1nstd229human GRCh38 chrX: 85,285,201-85,290,600 , GRCh37.p13 chrX: 84,540,207-84,545,606 POF1B
    nsv7090047copy number variation1nstd229human GRCh38 chrX: 85,285,101-85,290,200 , GRCh37.p13 chrX: 84,540,107-84,545,206 POF1B
    nsv7090046copy number variation1nstd229human GRCh38 chrX: 85,276,201-85,283,600 , GRCh37.p13 chrX: 84,531,207-84,538,606 POF1B
    nsv7090045copy number variation1nstd229human GRCh38 chrX: 85,276,201-85,282,900 , GRCh37.p13 chrX: 84,531,207-84,537,906 POF1B
    nsv7090044copy number variation1nstd229human GRCh38 chrX: 85,276,201-85,280,100 , GRCh37.p13 chrX: 84,531,207-84,535,106 POF1B
    nsv7090043copy number variation1nstd229human GRCh38 chrX: 85,276,156-85,276,674 , GRCh37.p13 chrX: 84,531,162-84,531,680 POF1B
    nsv7090042copy number variation1nstd229human GRCh38 chrX: 85,276,101-85,282,600 , GRCh37.p13 chrX: 84,531,107-84,537,606 POF1B
    nsv7090041copy number variation1nstd229human GRCh38 chrX: 85,276,101-85,279,500 , GRCh37.p13 chrX: 84,531,107-84,534,506 POF1B
    nsv7055976inversion1nstd229human GRCh38 chrX: 85,326,944-85,328,903 , GRCh37.p13 chrX: 84,581,950-84,583,909 POF1B
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