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Items: 1 to 20 of 230

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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
    nsv7077704inversion1nstd229human GRCh38 chr11: 300,985-327,365 , GRCh37.p13 chr11: 300,985-327,365 IFITM3, IFITM2, 2 more genes
    nsv7077499inversion1nstd229human GRCh38 chr11: 309,077-319,972 , GRCh37.p13 chr11: 309,077-319,972 IFITM2, IFITM3, 1 more genes
    nsv7076127inversion1nstd229human GRCh38 chr11: 313,426-337,283 , GRCh37.p13 chr11: 313,426-337,283 IFITM3, LOC105376505, 1 more genes
    nsv7076031inversion1nstd229human GRCh38 chr11: 309,083-319,963 , GRCh37.p13 chr11: 309,083-319,963 IFITM3, IFITM1, 1 more genes
    nsv7074423inversion1nstd229human GRCh38 chr11: 318,993-337,650 , GRCh37.p13 chr11: 318,993-337,650 LOC105376505, IFITM3
    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
    nsv7063095inversion1nstd229human GRCh38 chr11: 316,979-343,250 , GRCh37.p13 chr11: 316,979-343,250 IFITM3, LOC105376505
    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
    nsv7060552inversion1nstd229human GRCh38 chr11: 312,498-374,044 , GRCh37.p13 chr11: 312,498-374,044 IFITM1, B4GALNT4, 2 more genes
    nsv7058407inversion1nstd229human GRCh38 chr11: 315,010-319,622 , GRCh37.p13 chr11: 315,010-319,622 IFITM3, IFITM1
    nsv6895505copy number variation1nstd229human GRCh38 chr11: 253,210-322,853 , GRCh37.p13 chr11: 253,210-322,853 COX8BP, PGGHG, 7 more genes
    nsv6894858copy number variation1nstd229human GRCh38 chr11: 319,501-349,500 , GRCh37.p13 chr11: 319,501-349,500 LOC105376505, IFITM3
    nsv6894024copy number variation1nstd229human GRCh38 chr11: 283,901-340,100 , GRCh37.p13 chr11: 283,901-340,100 NLRP6, IFITM5, 6 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
    nsv6621157copy number variation1nstd224human GRCh37 chr11: 307,036-345,595 , GRCh38.p12 chr11: 307,036-345,595 IFITM3, LOC105376505, 2 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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