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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5650443insertion1nstd207human GRCh38 chr11: 800,486-800,486 , GRCh37.p13 chr11: 800,486-800,486 PIDD1
    nsv5590320copy number variation1nstd207human GRCh38 chr11: 801,741-801,792 , GRCh37.p13 chr11: 801,741-801,792 PIDD1
    nsv5562677inversion1nstd206human GRCh38 chr11: 806,073-806,777 , GRCh37.p13 chr11: 806,073-806,777 PIDD1
    nsv5504702copy number variation1nstd206human GRCh38 chr11: 805,892-807,044 , GRCh37.p13 chr11: 805,892-807,044 PIDD1
    nsv5497393copy number variation1nstd206human GRCh38 chr11: 800,432-800,523 , GRCh37.p13 chr11: 800,432-800,523 PIDD1
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5317479copy number variation1nstd204human GRCh38.p13 chr11: 708,633-1,150,137 , GRCh37.p13 chr11: 708,633-1,144,045 MUC2, CRACR2B, 21 more genes
    nsv5258461copy number variation1nstd204human GRCh38.p13 chr11: 520,301-974,900 , GRCh37.p13 chr11: 520,301-974,900 , SCT, 33 more genes
    nsv5242369copy number variation1nstd204human GRCh37.p13 chr11: 800,301-881,400 , GRCh38.p13 chr11: 800,301-881,400 CD151, POLR2L, 7 more genes
    nsv5130835mobile element insertion1nstd203human GRCh38 chr11: 806,761-806,780 , GRCh37.p13 chr11: 806,761-806,780 PIDD1
    nsv4984101copy number variation1nstd200human GRCh38 chr11: 708,641-1,150,129 , GRCh37.p13 chr11: 708,641-1,144,037 POLR2L, MUC6, 21 more genes
    nsv4984100copy number variation1nstd200human GRCh38 chr11: 642,551-894,927 , GRCh37.p13 chr11: 642,551-894,927 EPS8L2, PNPLA2, 17 more genes
    nsv4977795copy number variation1nstd200human GRCh38 chr11: 809,401-809,475 , GRCh37.p13 chr11: 809,401-809,475 PIDD1, RPLP2
    nsv4843772copy number variation1nstd200human GRCh37 chr11: 708,641-1,144,037 , GRCh38.p12 chr11|NT_187681.1: 1-218,430 , GRCh38.p12 chr11: 708,641-1,150,129 SLC25A22, PANO1, 21 more genes
    nsv4836915copy number variation1nstd200human GRCh37 chr11: 642,551-894,927 , GRCh38.p12 chr11: 642,551-894,927 CHID1, PANO1, 17 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4729665copy number variation1nstd102humanUncertain significance GRCh37 chr11: 230,615-1,150,353 , GRCh38.p12 chr11: 230,615-1,156,726 CD151, RPLP2, 57 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4681827copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755 LOC105376517, KRTAP5-2, 99 more genes
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