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Items: 1 to 20 of 314

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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
    nsv7094110copy number variation1nstd102humanUncertain significance GRCh37 chr11: 822,584-827,508 , GRCh38.p12 chr11: 822,584-827,508 PNPLA2, CRACR2B
    nsv7093693copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,636-819,925 , GRCh38.p12 chr11: 532,636-819,925 , GRCh38.p12 chr11|NT_187586.1: 62,277-209,248 HRAS, LRRC56, 25 more genes
    nsv7068164inversion1nstd229human GRCh38 chr11: 525,138-982,890 , GRCh37.p13 chr11: 525,138-982,890 DRD4, LMNTD2-AS1, 32 more genes
    nsv6889153copy number variation1nstd229human GRCh38 chr11: 814,801-818,700 , GRCh37.p13 chr11: 814,801-818,700 PNPLA2
    nsv6884289copy number variation1nstd229human GRCh38 chr11: 814,827-818,678 , GRCh37.p13 chr11: 814,827-818,678 PNPLA2
    nsv6880816copy number variation1nstd229human GRCh38 chr11: 694,601-1,110,400 , GRCh37.p13 chr11: 694,601-1,104,308 TALDO1, CD151, 23 more genes
    nsv6880651copy number variation1nstd229human GRCh38 chr11: 821,003-824,680 , GRCh37.p13 chr11: 821,003-824,680 CRACR2B, PNPLA2
    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
    nsv6621268copy number variation1nstd224human GRCh37 chr11: 823,729-836,407 , GRCh38.p12 chr11: 823,729-836,407 PNPLA2, CD151, 1 more genes
    nsv6450007copy number variation1nstd223human GRCh38 chr11: 642,551-894,924 , GRCh37.p13 chr11: 642,551-894,924 PANO1, SLC25A22, 17 more genes
    nsv6447012copy number variation1nstd223human GRCh38 chr11: 815,666-817,419 , GRCh37.p13 chr11: 815,666-817,419 PNPLA2
    nsv6446059copy number variation1nstd223human GRCh38 chr11: 814,827-818,673 , GRCh37.p13 chr11: 814,827-818,673 PNPLA2
    nsv6442745copy number variation1nstd223human GRCh38 chr11: 699,104-843,498 , GRCh37.p13 chr11: 699,104-843,498 TMEM80, PNPLA2, 16 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
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6309452copy number variation1nstd102humanUncertain significance GRCh37 chr11: 819,719-822,626 , GRCh38.p12 chr11: 819,719-822,626 PNPLA2
    nsv6309282copy number variation1nstd102humanUncertain significance GRCh37 chr11: 678,674-838,192 , GRCh38.p12 chr11: 678,674-838,192 CRACR2B, PNPLA2, 15 more genes
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