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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148129copy number variation1nstd102humanPathogenic GRCh37 chr9: 77,112,742-77,113,051 , GRCh38.p12 chr9: 74,497,826-74,498,135 RORB, RORB-AS1
    nsv7072214inversion1nstd229human GRCh38 chr9: 74,500,209-74,500,322 , GRCh37.p13 chr9: 77,115,125-77,115,238 RORB
    nsv7070259inversion1nstd229human GRCh38 chr9: 74,677,595-74,697,520 , GRCh37.p13 chr9: 77,292,511-77,312,436 RORB
    nsv7068500inversion1nstd229human GRCh38 chr9: 74,672,285-74,682,364 , GRCh37.p13 chr9: 77,287,201-77,297,280 RORB
    nsv6876635copy number variation1nstd229human GRCh38 chr9: 72,384,161-74,793,192 , GRCh37.p13 chr9: 74,999,077-77,408,108 LOC101927329, LOC100289351, 27 more genes
    nsv6873860copy number variation1nstd229human GRCh38 chr9: 74,629,610-74,629,983 , GRCh37.p13 chr9: 77,244,526-77,244,899 RORB, LOC105376088
    nsv6873821copy number variation1nstd229human GRCh38 chr9: 74,521,668-74,521,773 , GRCh37.p13 chr9: 77,136,584-77,136,689 RORB
    nsv6872996copy number variation1nstd229human GRCh38 chr9: 74,617,342-74,620,304 , GRCh37.p13 chr9: 77,232,258-77,235,220 RORB
    nsv6871364copy number variation1nstd229human GRCh38 chr9: 74,550,376-74,556,877 , GRCh37.p13 chr9: 77,165,292-77,171,793 RORB
    nsv6869717copy number variation1nstd229human GRCh38 chr9: 74,542,956-74,546,553 , GRCh37.p13 chr9: 77,157,872-77,161,469 RORB
    nsv6868408copy number variation1nstd229human GRCh38 chr9: 74,551,252-74,551,316 , GRCh37.p13 chr9: 77,166,168-77,166,232 RORB
    nsv6867730copy number variation1nstd229human GRCh38 chr9: 74,632,232-74,632,835 , GRCh37.p13 chr9: 77,247,148-77,247,751 RORB, LOC105376088
    nsv6867723copy number variation1nstd229human GRCh38 chr9: 74,637,301-74,645,400 , GRCh37.p13 chr9: 77,252,217-77,260,316 RORB, LOC105376088
    nsv6867601copy number variation1nstd229human GRCh38 chr9: 74,649,401-74,866,500 , GRCh37.p13 chr9: 77,264,317-77,481,416 RN7SKP47, RNY4P1, 4 more genes
    nsv6859693copy number variation1nstd229human GRCh38 chr9: 74,269,541-74,698,518 , GRCh37.p13 chr9: 76,884,457-77,313,434 RORB, RORB-AS1, 4 more genes
    nsv6859243copy number variation1nstd229human GRCh38 chr9: 74,613,776-74,623,337 , GRCh37.p13 chr9: 77,228,692-77,238,253 RORB
    nsv6858646copy number variation1nstd229human GRCh38 chr9: 74,672,301-74,677,600 , GRCh37.p13 chr9: 77,287,217-77,292,516 RORB
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6574274inversion1nstd223human GRCh38 chr9: 74,591,938-74,592,732 , GRCh37.p13 chr9: 77,206,854-77,207,648 RORB
    nsv6573839inversion1nstd223human GRCh38 chr9: 74,549,339-74,549,915 , GRCh37.p13 chr9: 77,164,255-77,164,831 RORB
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