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Items: 1 to 20 of 177

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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
    nsv7093458delins1nstd102humanLikely benign GRCh37 chr11: 2,906,120-2,906,187 , GRCh38 chr11: 2,884,890-2,884,957 CDKN1C
    nsv7093426delins1nstd102humanLikely benign GRCh37 chr11: 2,906,093-2,906,094 , GRCh38 chr11: 2,884,863-2,884,864 CDKN1C
    nsv7093343copy number variation1nstd102humanLikely benign GRCh38 chr11: 2,884,942-2,885,007 , GRCh37 chr11: 2,906,172-2,906,237 CDKN1C
    nsv7093150copy number variation1nstd102humanLikely benign GRCh37 chr11: 2,906,100-2,906,165 , GRCh38 chr11: 2,884,870-2,884,935 CDKN1C
    nsv7093037copy number variation1nstd102humanLikely benign GRCh37 chr11: 2,906,166-2,906,243 , GRCh38 chr11: 2,884,936-2,885,013 CDKN1C
    nsv6917469copy number variation1nstd229human GRCh38 chr11: 2,867,748-2,894,423 , GRCh37.p13 chr11: 2,888,978-2,915,653 SLC22A18AS, KCNQ1DN, 1 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6913592copy number variation1nstd229human GRCh38 chr11: 2,838,203-2,957,732 , GRCh37.p13 chr11: 2,859,433-2,978,962 KCNQ1, PHLDA2, 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
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 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
    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
    nsv6315544copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,314,240-2,915,570 , GRCh38.p12 chr11: 2,293,010-2,894,340 COX6CP18, SLC22A18AS, 14 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
    nsv6314680copy number variation1nstd102humanLikely benign GRCh37 chr11: 2,906,178-2,906,237 , GRCh38 chr11: 2,884,948-2,885,007 CDKN1C
    nsv6314679copy number variation1nstd102humanLikely benign GRCh38 chr11: 2,884,931-2,884,984 , GRCh37 chr11: 2,906,161-2,906,214 CDKN1C
    nsv6314678copy number variation1nstd102humanLikely benign GRCh37 chr11: 2,906,149-2,906,226 , GRCh38 chr11: 2,884,919-2,884,996 CDKN1C
    nsv6314677copy number variation1nstd102humanLikely benign GRCh37 chr11: 2,906,149-2,906,214 , GRCh38 chr11: 2,884,919-2,884,984 CDKN1C
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