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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7059966inversion1nstd229human GRCh38 chr11: 1,040,450-1,150,902 , GRCh37.p13 chr11: 1,040,450-1,144,813 LINC02688, MUC2, 1 more genes
    nsv6891876copy number variation1nstd229human GRCh38 chr11: 1,032,046-1,119,580 , GRCh37.p13 chr11: 1,032,046-1,113,488 MUC6, LINC02688, 2 more genes
    nsv6887896copy number variation1nstd229human GRCh38 chr11: 1,021,613-1,262,743 , GRCh37.p13 chr11: 1,021,613-1,283,973 MUC5B, MUC5AC, 6 more genes
    nsv6886469copy number variation1nstd229human GRCh38 chr11: 1,051,780-1,051,805 , GRCh37.p13 chr11: 1,051,780-1,051,805 LINC02688
    nsv6881940copy number variation1nstd229human GRCh38 chr11: 978,901-1,098,200 , GRCh37.p13 chr11: 978,901-1,075,386 MUC6, LOC107987157, 3 more genes
    nsv6880816copy number variation1nstd229human GRCh38 chr11: 694,601-1,110,400 , GRCh37.p13 chr11: 694,601-1,104,308 TALDO1, CD151, 23 more genes
    nsv6880504copy number variation1nstd229human GRCh38 chr11: 1,050,634-1,050,696 , GRCh37.p13 chr11: 1,050,634-1,050,696 LINC02688
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6621272copy number variation1nstd224human GRCh37 chr11: 836,406-1,282,678 , GRCh38.p12 chr11: 836,406-1,261,448 TSPAN4, CHID1, 12 more genes
    nsv6446694copy number variation1nstd223human GRCh38 chr11: 1,055,658-1,056,044 , GRCh37.p13 chr11: 1,055,658-1,056,044 LINC02688
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6032905copy number variation1nstd212human GRCh38 chr11: 1,055,658-1,056,044 , GRCh37.p13 chr11: 1,055,658-1,056,044 LINC02688
    nsv5919324copy number variation1nstd209human GRCh38 chr11: 1,055,658-1,056,043 , GRCh37.p13 chr11: 1,055,658-1,056,043 LINC02688
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5507196copy number variation1nstd206human GRCh38 chr11: 1,055,659-1,056,044 , GRCh37.p13 chr11: 1,055,659-1,056,044 LINC02688
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