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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094372copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,691,680-42,703,981 , GRCh38.p12 chr15: 42,399,482-42,411,783 ZNF106, CAPN3
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6976027copy number variation1nstd229human GRCh38 chr15: 42,464,116-42,464,192 , GRCh37.p13 chr15: 42,756,314-42,756,390 ZNF106
    nsv6974969copy number variation1nstd229human GRCh38 chr15: 42,414,301-42,438,500 , GRCh37.p13 chr15: 42,706,499-42,730,698 RNU6-188P, ZNF106
    nsv6973880copy number variation1nstd229human GRCh38 chr15: 42,428,826-42,431,456 , GRCh37.p13 chr15: 42,721,024-42,723,654 ZNF106
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6972241copy number variation1nstd229human GRCh38 chr15: 42,481,301-42,591,500 , GRCh37.p13 chr15: 42,773,499-42,883,698 EIF4EBP2P2, STARD9, 5 more genes
    nsv6970347copy number variation1nstd229human GRCh38 chr15: 42,267,286-42,589,151 , GRCh37.p13 chr15: 42,559,484-42,881,349 LRRC57, GANC, 11 more genes
    nsv6970216copy number variation1nstd229human GRCh38 chr15: 42,430,909-42,433,252 , GRCh37.p13 chr15: 42,723,107-42,725,450 ZNF106
    nsv6968947copy number variation1nstd229human GRCh38 chr15: 42,396,863-42,531,333 , GRCh37.p13 chr15: 42,689,061-42,823,531 SNAP23, RNU6-188P, 3 more genes
    nsv6968879copy number variation1nstd229human GRCh38 chr15: 42,339,484-42,411,959 , GRCh37.p13 chr15: 42,631,682-42,704,157 ZNF106, CAPN3, 2 more genes
    nsv6965479copy number variation1nstd229human GRCh38 chr15: 42,416,601-42,427,400 , GRCh37.p13 chr15: 42,708,799-42,719,598 ZNF106, RNU6-188P
    nsv6963002copy number variation1nstd229human GRCh38 chr15: 42,416,902-42,416,921 , GRCh37.p13 chr15: 42,709,100-42,709,119 ZNF106
    nsv6636133copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,651,994-42,703,999 , GRCh38.p12 chr15: 42,359,796-42,411,801 ZNF106, LOC105370794, 1 more genes
    nsv6593125inversion1nstd223human GRCh38 chr15: 42,462,475-42,463,091 , GRCh37.p13 chr15: 42,754,673-42,755,289 ZNF106
    nsv6591326inversion1nstd223human GRCh38 chr15: 42,478,749-42,479,579 , GRCh37.p13 chr15: 42,770,947-42,771,777 ZNF106
    nsv6584296inversion1nstd223human GRCh38 chr15: 42,477,688-42,478,269 , GRCh37.p13 chr15: 42,769,886-42,770,467 ZNF106
    nsv6583531inversion1nstd223human GRCh38 chr15: 42,452,256-42,452,727 , GRCh37.p13 chr15: 42,744,454-42,744,925 ZNF106
    nsv6579845inversion1nstd223human GRCh38 chr15: 42,428,825-42,429,314 , GRCh37.p13 chr15: 42,721,023-42,721,512 ZNF106
    nsv6579137inversion1nstd223human GRCh38 chr15: 42,423,105-42,423,581 , GRCh37.p13 chr15: 42,715,303-42,715,779 ZNF106
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