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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137204copy number variation1nstd102humanPathogenic GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873 PKP3, RN7SL838P, 32 more genes
    nsv7068392inversion1nstd229human GRCh38 chr11: 260,223-620,051 , GRCh37.p13 chr11: 260,223-620,051 MIR210, LMNTD2-AS1, 25 more genes
    nsv7067944inversion1nstd229human GRCh38 chr11: 288,558-695,861 , GRCh37.p13 chr11: 288,558-695,861 IRF7, TMEM80, 28 more genes
    nsv7067338inversion1nstd229human GRCh38 chr11: 286,347-286,368 , GRCh37.p13 chr11: 286,347-286,368 PGGHG, NLRP6
    nsv7061086inversion1nstd229human GRCh38 chr11: 295,389-324,779 , GRCh37.p13 chr11: 295,389-324,779 IFITM3, IFITM2, 4 more genes
    nsv7060764inversion1nstd229human GRCh38 chr11: 214,534-319,607 , GRCh37.p13 chr11: 214,534-319,607 IFITM1, MRPS24P1, 10 more genes
    nsv6895505copy number variation1nstd229human GRCh38 chr11: 253,210-322,853 , GRCh37.p13 chr11: 253,210-322,853 COX8BP, PGGHG, 7 more genes
    nsv6894024copy number variation1nstd229human GRCh38 chr11: 283,901-340,100 , GRCh37.p13 chr11: 283,901-340,100 NLRP6, IFITM5, 6 more genes
    nsv6893143copy number variation1nstd229human GRCh38 chr11: 288,153-288,194 , GRCh37.p13 chr11: 288,153-288,194 PGGHG
    nsv6892897copy number variation1nstd229human GRCh38 chr11: 279,301-289,400 , GRCh37.p13 chr11: 279,301-289,400 PGGHG, NLRP6
    nsv6891971copy number variation1nstd229human GRCh38 chr11: 283,503-298,474 , GRCh37.p13 chr11: 283,503-298,474 PGGHG, NLRP6, 1 more genes
    nsv6886651copy number variation1nstd229human GRCh38 chr11: 267,480-294,285 , GRCh37.p13 chr11: 267,480-294,285 NLRP6, PGGHG
    nsv6883694copy number variation1nstd229human GRCh38 chr11: 209,042-305,543 , GRCh37.p13 chr11: 209,042-305,543 MRPS24P1, PGGHG, 8 more genes
    nsv6883267copy number variation1nstd229human GRCh38 chr11: 272,722-295,528 , GRCh37.p13 chr11: 272,722-295,528 PGGHG, NLRP6
    nsv6879558copy number variation1nstd229human GRCh38 chr11: 293,104-312,009 , GRCh37.p13 chr11: 293,104-312,009 PGGHG, IFITM2, 2 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6635428copy number variation1nstd227human GRCh37 chr11: 198,510-356,090 , GRCh38.p12 chr11: 198,510-356,090 PSMD13, IFITM1, 14 more genes
    nsv6621079copy number variation1nstd224human GRCh37 chr11: 270,715-290,901 , GRCh38.p12 chr11: 270,715-290,901 PGGHG, NLRP6
    nsv6620972copy number variation1nstd224human GRCh37 chr11: 197,350-316,299 , GRCh38.p12 chr11: 197,350-316,299 PSMD13, SIRT3, 12 more genes
    nsv6620915copy number variation1nstd224human GRCh37 chr11: 241,523-345,595 , GRCh38.p12 chr11: 241,523-345,595 IFITM3, LOC105376505, 9 more genes
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