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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921168copy number variation1nstd209human GRCh38 chr11: 263,081-280,481 , GRCh37.p13 chr11: 263,081-280,481 NLRP6
    nsv5910989copy number variation1nstd209human GRCh38 chr11: 264,259-295,382 , GRCh37.p13 chr11: 264,259-295,382 PGGHG, NLRP6
    nsv5867415copy number variation2nstd209human GRCh38 chr11: 263,982-280,711 , GRCh37.p13 chr11: 263,982-280,711 NLRP6
    nsv5865510copy number variation2nstd209human GRCh38 chr11: 277,828-280,527 , GRCh37.p13 chr11: 277,828-280,527 NLRP6
    nsv5859764copy number variation1nstd209human GRCh38 chr11: 280,128-285,510 , GRCh37.p13 chr11: 280,128-285,510 NLRP6
    nsv5852195copy number variation1nstd209human GRCh38 chr11: 283,811-286,410 , GRCh37.p13 chr11: 283,811-286,410 NLRP6, PGGHG
    nsv5495750copy number variation1nstd206human GRCh38 chr11: 275,863-277,727 , GRCh37.p13 chr11: 275,863-277,727 NLRP6
    nsv5305034copy number variation1nstd204human GRCh38.p13 chr11: 284,497-285,620 , GRCh37.p13 chr11: 284,497-285,620 NLRP6
    nsv5260014copy number variation1nstd204human GRCh38.p13 chr11: 224,101-321,400 , GRCh37.p13 chr11: 224,101-321,400 PSMD13, NLRP6, 9 more genes
    nsv5259448copy number variation1nstd204human GRCh38.p13 chr11: 284,501-285,600 , GRCh37.p13 chr11: 284,501-285,600 NLRP6
    nsv5259145copy number variation1nstd204human GRCh38.p13 chr11: 192,201-519,400 , GRCh37.p13 chr11: 192,201-519,400 , SIGIRR, 25 more genes
    nsv4984089copy number variation1nstd200human GRCh38 chr11: 253,210-322,854 , GRCh37.p13 chr11: 253,210-322,854 IFITM1, PGGHG, 7 more genes
    nsv4977754copy number variation1nstd200human GRCh38 chr11: 284,507-285,617 , GRCh37.p13 chr11: 284,507-285,617 NLRP6
    nsv4977753copy number variation1nstd200human GRCh38 chr11: 267,479-294,284 , GRCh37.p13 chr11: 267,479-294,284 NLRP6, PGGHG
    nsv4841359copy number variation1nstd200human GRCh37 chr11: 267,600-294,284 , GRCh38.p12 chr11: 267,600-294,284 PGGHG, NLRP6
    nsv4836740copy number variation1nstd200human GRCh37 chr11: 284,507-285,617 , GRCh38.p12 chr11: 284,507-285,617 NLRP6
    nsv4774871mobile element deletion1nstd200human GRCh37 chr11: 283,313-283,611 , GRCh38.p12 chr11: 283,313-283,611 NLRP6
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4729665copy number variation1nstd102humanUncertain significance GRCh37 chr11: 230,615-1,150,353 , GRCh38.p12 chr11: 230,615-1,156,726 CD151, RPLP2, 57 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
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