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Items: 1 to 20 of 951

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147895insertion1nstd232human GRCh37.p13 chrX: 91,666,955-91,666,955 , GRCh38.p12 chrX: 92,411,956-92,411,956 PCDH11X
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7092792copy number variation1nstd229human GRCh38 chrX: 92,545,501-92,579,400 , GRCh37.p13 chrX: 91,800,500-91,834,399 PCDH11X
    nsv7092791copy number variation1nstd229human GRCh38 chrX: 92,503,463-92,503,600 , GRCh37.p13 chrX: 91,758,462-91,758,599 PCDH11X
    nsv7092790copy number variation1nstd229human GRCh38 chrX: 92,501,501-92,505,400 , GRCh37.p13 chrX: 91,756,500-91,760,399 PCDH11X
    nsv7092789copy number variation1nstd229human GRCh38 chrX: 92,434,573-92,434,821 , GRCh37.p13 chrX: 91,689,572-91,689,820 PCDH11X
    nsv7092788copy number variation1nstd229human GRCh38 chrX: 92,414,762-92,414,838 , GRCh37.p13 chrX: 91,669,761-91,669,837 PCDH11X
    nsv7092787copy number variation1nstd229human GRCh38 chrX: 92,393,889-92,396,554 , GRCh37.p13 chrX: 91,648,888-91,651,553 PCDH11X
    nsv7092786copy number variation1nstd229human GRCh38 chrX: 92,311,701-92,314,300 , GRCh37.p13 chrX: 91,566,700-91,569,299 PCDH11X
    nsv7092785copy number variation1nstd229human GRCh38 chrX: 92,289,556-92,289,626 , GRCh37.p13 chrX: 91,544,555-91,544,625 PCDH11X
    nsv7092784copy number variation1nstd229human GRCh38 chrX: 92,228,420-92,571,076 , GRCh37.p13 chrX: 91,483,419-91,826,075 SNX3P1X, KRT18P11, 1 more genes
    nsv7092783copy number variation1nstd229human GRCh38 chrX: 92,223,501-92,250,900 , GRCh37.p13 chrX: 91,478,500-91,505,899 PCDH11X
    nsv7092782copy number variation1nstd229human GRCh38 chrX: 92,210,068-92,214,737 , GRCh37.p13 chrX: 91,465,067-91,469,736 PCDH11X
    nsv7092781copy number variation1nstd229human GRCh38 chrX: 92,193,301-92,196,600 , GRCh37.p13 chrX: 91,448,300-91,451,599 PCDH11X
    nsv7092780copy number variation1nstd229human GRCh38 chrX: 92,181,188-92,235,994 , GRCh37.p13 chrX: 91,436,187-91,490,993 PCDH11X
    nsv7092779copy number variation1nstd229human GRCh38 chrX: 92,180,911-92,187,804 , GRCh37.p13 chrX: 91,435,910-91,442,803 PCDH11X
    nsv7092778copy number variation1nstd229human GRCh38 chrX: 92,180,101-92,190,400 , GRCh37.p13 chrX: 91,435,100-91,445,399 PCDH11X
    nsv7092777copy number variation1nstd229human GRCh38 chrX: 92,180,101-92,183,500 , GRCh37.p13 chrX: 91,435,100-91,438,499 PCDH11X
    nsv7092776copy number variation1nstd229human GRCh38 chrX: 92,177,396-92,186,593 , GRCh37.p13 chrX: 91,432,395-91,441,592 PCDH11X
    nsv7092775copy number variation1nstd229human GRCh38 chrX: 92,150,050-92,184,754 , GRCh37.p13 chrX: 91,405,049-91,439,753 PCDH11X
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