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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137183copy number variation1nstd102humanPathogenic GRCh37 chr11: 2,683,186-2,683,314 , GRCh38.p12 chr11: 2,661,956-2,662,084 KCNQ1OT1, KCNQ1
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7094163copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,549,148-2,683,321 , GRCh38.p12 chr11: 2,527,918-2,662,091 KCNQ1OT1, KCNQ1
    nsv7093846copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 2,629,548-2,721,238 , GRCh38.p12 chr11: 2,608,318-2,700,008 KCNQ1, KCNQ1OT1
    nsv7093845copy number variation1nstd102humanPathogenic GRCh37 chr11: 2,466,329-2,869,233 , GRCh38.p12 chr11: 2,445,099-2,848,003 COX6CP18, KCNQ1, 2 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
    nsv7072778inversion1nstd229human GRCh38 chr11: 2,602,398-2,613,291 , GRCh37.p13 chr11: 2,623,628-2,634,521 KCNQ1OT1, KCNQ1
    nsv6917856copy number variation1nstd229human GRCh38 chr11: 2,676,689-2,679,666 , GRCh37.p13 chr11: 2,697,919-2,700,896 KCNQ1, KCNQ1OT1
    nsv6917303copy number variation1nstd229human GRCh38 chr11: 2,669,525-2,671,124 , GRCh37.p13 chr11: 2,690,755-2,692,354 KCNQ1, KCNQ1OT1
    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
    nsv6915487copy number variation1nstd229human GRCh38 chr11: 2,684,601-2,736,300 , GRCh37.p13 chr11: 2,705,831-2,757,530 KCNQ1, KCNQ1OT1
    nsv6911875copy number variation1nstd229human GRCh38 chr11: 2,667,891-2,671,037 , GRCh37.p13 chr11: 2,689,121-2,692,267 KCNQ1, KCNQ1OT1
    nsv6909713copy number variation1nstd229human GRCh38 chr11: 2,672,078-2,675,085 , GRCh37.p13 chr11: 2,693,308-2,696,315 KCNQ1, KCNQ1OT1
    nsv6909220copy number variation1nstd229human GRCh38 chr11: 2,673,782-2,673,884 , GRCh37.p13 chr11: 2,695,012-2,695,114 KCNQ1OT1, KCNQ1
    nsv6905139copy number variation1nstd229human GRCh38 chr11: 2,624,048-2,629,375 , GRCh37.p13 chr11: 2,645,278-2,650,605 KCNQ1OT1, KCNQ1
    nsv6904115copy number variation1nstd229human GRCh38 chr11: 2,691,001-2,693,300 , GRCh37.p13 chr11: 2,712,231-2,714,530 KCNQ1OT1, KCNQ1
    nsv6901914copy number variation1nstd229human GRCh38 chr11: 2,592,479-2,621,406 , GRCh37.p13 chr11: 2,613,709-2,642,636 KCNQ1, KCNQ1OT1
    nsv6901626copy number variation1nstd229human GRCh38 chr11: 2,601,096-2,606,666 , GRCh37.p13 chr11: 2,622,326-2,627,896 KCNQ1, KCNQ1OT1
    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
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