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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
    nsv7067672inversion1nstd229human GRCh38 chr11: 1,035,564-1,039,326 , GRCh37.p13 chr11: 1,035,564-1,039,326 MUC6
    nsv6892152copy number variation1nstd229human GRCh38 chr11: 1,035,562-1,038,517 , GRCh37.p13 chr11: 1,035,562-1,038,517 MUC6
    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
    nsv6888827copy number variation1nstd229human GRCh38 chr11: 997,819-1,042,551 , GRCh37.p13 chr11: 997,819-1,042,551 AP2A2, MUC6
    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
    nsv6887395copy number variation1nstd229human GRCh38 chr11: 1,030,158-1,034,090 , GRCh37.p13 chr11: 1,030,158-1,034,090 MUC6
    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
    nsv6880234copy number variation1nstd229human GRCh38 chr11: 1,026,901-1,031,300 , GRCh37.p13 chr11: 1,026,901-1,031,300 MUC6
    nsv6879404copy number variation1nstd229human GRCh38 chr11: 961,164-1,022,637 , GRCh37.p13 chr11: 961,164-1,022,637 MUC6, AP2A2
    nsv6878729copy number variation1nstd229human GRCh38 chr11: 1,023,357-1,023,431 , GRCh37.p13 chr11: 1,023,357-1,023,431 MUC6
    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
    nsv6636189copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,017,464-1,017,602 , GRCh38 chr11: 1,017,464-1,017,602 MUC6
    nsv6636149copy number variation1nstd102humanPathogenic GRCh38 chr11: 1,017,470-1,017,605 , GRCh37 chr11: 1,017,470-1,017,605 MUC6
    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
    nsv6446791copy number variation1nstd223human GRCh38 chr11: 1,018,054-1,018,696 , GRCh37.p13 chr11: 1,018,054-1,018,696 MUC6
    nsv6444494copy number variation1nstd223human GRCh38 chr11: 1,016,601-1,024,200 , GRCh37.p13 chr11: 1,016,601-1,024,200 MUC6
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