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Items: 1 to 20 of 354

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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
    nsv7093761copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489 TOLLIP-DT, KRTAP5-6, 58 more genes
    nsv6897386copy number variation1nstd229human GRCh38 chr11: 1,223,501-1,230,100 , GRCh37.p13 chr11: 1,244,731-1,251,330 MUC5B
    nsv6890403copy number variation1nstd229human GRCh38 chr11: 1,246,728-1,254,121 , GRCh37.p13 chr11: 1,267,958-1,275,351 MUC5B-AS1, MUC5B
    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
    nsv6887797copy number variation1nstd229human GRCh38 chr11: 1,155,001-1,235,300 , GRCh37.p13 chr11: 1,148,888-1,256,530 MUC5B, MUC5AC
    nsv6887750copy number variation1nstd229human GRCh38 chr11: 1,075,859-1,349,364 , GRCh37.p13 chr11: 1,099,880-1,370,594 TOLLIP, MIR6744, 6 more genes
    nsv6885276copy number variation1nstd229human GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693 KRTAP5-1, MIR675, 69 more genes
    nsv6881675copy number variation1nstd229human GRCh38 chr11: 1,247,001-1,248,000 , GRCh37.p13 chr11: 1,268,231-1,269,230 MUC5B-AS1, MUC5B
    nsv6880847copy number variation1nstd229human GRCh38 chr11: 1,242,601-1,251,100 , GRCh37.p13 chr11: 1,263,831-1,272,330 MUC5B, MUC5B-AS1
    nsv6880077copy number variation1nstd229human GRCh38 chr11: 1,246,616-1,248,298 , GRCh37.p13 chr11: 1,267,846-1,269,528 MUC5B-AS1, MUC5B
    nsv6879718copy number variation1nstd229human GRCh38 chr11: 1,203,314-1,714,253 , GRCh37.p13 chr11: 1,224,544-1,735,483 KRTAP5-3, KRTAP5-2, 17 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
    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
    nsv6454357copy number variation1nstd223human GRCh38 chr11: 1,248,028-1,249,745 , GRCh37.p13 chr11: 1,269,258-1,270,975 MUC5B, MUC5B-AS1
    nsv6453922copy number variation1nstd223human GRCh38 chr11: 1,242,656-1,245,956 , GRCh37.p13 chr11: 1,263,886-1,267,186 MUC5B, MUC5B-AS1
    nsv6452065copy number variation1nstd223human GRCh38 chr11: 1,250,901-1,251,400 , GRCh37.p13 chr11: 1,272,131-1,272,630 MUC5B
    nsv6449669copy number variation1nstd223human GRCh38 chr11: 1,245,701-1,247,300 , GRCh37.p13 chr11: 1,266,931-1,268,530 MUC5B, MUC5B-AS1
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