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Items: 1 to 20 of 718

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143428copy number variation1nstd232human GRCh37.p13 chrX: 3,609,471-3,609,525 , GRCh38.p12 chrX: 3,691,430-3,691,484 PRKX
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098867copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773 RPL14P5, NLGN4X, 64 more genes
    nsv7076649copy number variation1nstd229human GRCh38 chrX: 3,691,432-3,691,488 , GRCh37.p13 chrX: 3,609,473-3,609,529 PRKX
    nsv7074528copy number variation1nstd229human GRCh38 chrX: 3,686,268-3,688,120 , GRCh37.p13 chrX: 3,604,309-3,606,161 PRKX
    nsv7074257copy number variation1nstd229human GRCh38 chrX: 3,689,257-3,697,354 , GRCh37.p13 chrX: 3,607,298-3,615,395 PRKX
    nsv7072818copy number variation1nstd229human GRCh38 chrX: 3,688,201-3,688,600 , GRCh37.p13 chrX: 3,606,242-3,606,641 PRKX
    nsv7069931copy number variation1nstd229human GRCh38 chrX: 3,689,674-4,270,789 , GRCh37.p13 chrX: 3,607,715-4,188,830 RPS27AP20, FAM239B, 8 more genes
    nsv7067713copy number variation1nstd229human GRCh38 chrX: 3,680,302-3,711,558 , GRCh37.p13 chrX: 3,598,343-3,629,599 PRKX
    nsv7062057copy number variation1nstd229human GRCh38 chrX: 3,666,593-3,666,772 , GRCh37.p13 chrX: 3,584,634-3,584,813 PRKX, PRKX-AS1
    nsv7060606copy number variation1nstd229human GRCh38 chrX: 3,680,314-3,738,839 , GRCh37.p13 chrX: 3,598,355-3,656,880 PRKX, RPS27AP20
    nsv7060536copy number variation1nstd229human GRCh38 chrX: 3,456,875-3,688,181 , GRCh37.p13 chrX: 3,374,916-3,606,222 SNORA48B, RNU6-114P, 3 more genes
    nsv7060144copy number variation1nstd229human GRCh38 chrX: 3,662,848-3,666,912 , GRCh37.p13 chrX: 3,580,889-3,584,953 PRKX, PRKX-AS1
    nsv7059872copy number variation1nstd229human GRCh38 chrX: 3,621,338-5,069,395 , GRCh37.p13 chrX: 3,539,379-4,987,436 FAM239B, FAM239C, 10 more genes
    nsv7059789copy number variation1nstd229human GRCh38 chrX: 3,642,424-3,646,121 , GRCh37.p13 chrX: 3,560,465-3,564,162 PRKX
    nsv7059366copy number variation1nstd229human GRCh38 chrX: 3,634,001-3,805,100 , GRCh37.p13 chrX: 3,552,042-3,723,141 PRKX-AS1, PRKX, 1 more genes
    nsv7059110copy number variation1nstd229human GRCh38 chrX: 3,685,074-3,703,768 , GRCh37.p13 chrX: 3,603,115-3,621,809 PRKX
    nsv7032790inversion1nstd229human GRCh38 chrX: 3,658,477-3,659,139 , GRCh37.p13 chrX: 3,576,518-3,577,180 PRKX-AS1, PRKX
    nsv6636165copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899 GPX1P1, XG, 108 more genes
    nsv6636029copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,626,596-7,832,236 , GRCh38.p12 chrX: 1,507,703-7,864,195 ARSL, FAM239A, 53 more genes
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