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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926120copy number variation1nstd209human GRCh38 chr9: 21,199,974-21,215,139 , GRCh37.p13 chr9: 21,199,973-21,215,138 IFNA7, IFNA10, 2 more genes
    nsv5920674copy number variation1nstd209human GRCh38 chr9: 21,195,856-21,214,402 , GRCh37.p13 chr9: 21,195,855-21,214,401 IFNA7, IFNA10, 2 more genes
    nsv5916420copy number variation1nstd209human GRCh38 chr9: 21,193,534-21,212,021 , GRCh37.p13 chr9: 21,193,533-21,212,020 IFNA7, IFNA10, 1 more genes
    nsv5912909copy number variation1nstd209human GRCh38 chr9: 21,185,712-21,205,287 , GRCh37.p13 chr9: 21,185,711-21,205,286 IFNA4, IFNA7, 2 more genes
    nsv5865495copy number variation2nstd209human GRCh38 chr9: 21,199,671-21,207,660 , GRCh37.p13 chr9: 21,199,670-21,207,659 IFNWP18, IFNA7, 1 more genes
    nsv5856094copy number variation2nstd209human GRCh38 chr9: 21,197,214-21,214,618 , GRCh37.p13 chr9: 21,197,213-21,214,617 IFNWP18, IFNA10, 2 more genes
    nsv5850244copy number variation1nstd209human GRCh38 chr9: 21,193,669-21,199,720 , GRCh37.p13 chr9: 21,193,668-21,199,719 IFNA7
    nsv5590833copy number variation1nstd207human GRCh38 chr9: 21,192,513-21,211,048 , GRCh37.p13 chr9: 21,192,512-21,211,047 IFNA7, IFNA10, 1 more genes
    nsv5490741copy number variation1nstd206human GRCh38 chr9: 21,196,132-21,214,660 , GRCh37.p13 chr9: 21,196,131-21,214,659 IFNA7, IFNA16, 2 more genes
    nsv5478587copy number variation1nstd206human GRCh38 chr9: 21,201,509-21,216,568 , GRCh37.p13 chr9: 21,201,508-21,216,567 IFNA16, IFNA10, 2 more genes
    nsv5311957copy number variation1nstd204human GRCh38.p13 chr9: 21,202,511-21,208,018 , GRCh37.p13 chr9: 21,202,510-21,208,017 IFNA10, IFNWP18, 1 more genes
    nsv5300556copy number variation1nstd204human GRCh37.p13 chr9: 21,193,529-21,212,063 , GRCh38.p13 chr9: 21,193,530-21,212,064 IFNA7, IFNA10, 1 more genes
    nsv5259224copy number variation1nstd204human GRCh38.p13 chr9: 21,191,338-21,209,902 , GRCh37.p13 chr9: 21,191,337-21,209,901 IFNWP9, IFNA7, 2 more genes
    nsv5253283copy number variation1nstd204human GRCh38.p13 chr9: 21,193,219-21,203,740 , GRCh37.p13 chr9: 21,193,218-21,203,739 IFNA7
    nsv5240688copy number variation1nstd204human GRCh38.p13 chr9: 21,202,219-21,207,660 , GRCh37.p13 chr9: 21,202,218-21,207,659 IFNWP18, IFNA7, 1 more genes
    nsv4963626copy number variation1nstd200human GRCh38 chr9: 21,200,495-21,215,599 , GRCh37.p13 chr9: 21,200,494-21,215,598 IFNWP18, IFNA10, 2 more genes
    nsv4963625copy number variation1nstd200human GRCh38 chr9: 21,199,942-21,215,073 , GRCh37.p13 chr9: 21,199,941-21,215,072 IFNWP18, IFNA7, 2 more genes
    nsv4963624copy number variation1nstd200human GRCh38 chr9: 21,199,905-21,204,231 , GRCh37.p13 chr9: 21,199,904-21,204,230 IFNA10, IFNA7
    nsv4963623copy number variation1nstd200human GRCh38 chr9: 21,193,447-21,212,168 , GRCh37.p13 chr9: 21,193,446-21,212,167 IFNA10, IFNWP18, 1 more genes
    nsv4963622copy number variation1nstd200human GRCh38 chr9: 21,192,552-21,211,100 , GRCh37.p13 chr9: 21,192,551-21,211,099 IFNA7, IFNWP18, 1 more genes
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