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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4678906copy number variation1nstd189human GRCh37.p13 chr11: 94,797,938-94,943,741 , GRCh38.p12 chr11: 95,064,774-95,210,577 SRSF8, ENDOD1, 3 more genes
    nsv4193086copy number variation1nstd166human GRCh37.p13 chr11: 94,793,143-94,898,836 , GRCh38.p12 chr11: 95,059,979-95,165,672 SESN3, LNCRNA-IUR, 3 more genes
    nsv3965229insertion1nstd168human GRCh38 chr11: 95,123,821-95,144,240 , GRCh37.p13 chr11: 94,856,985-94,877,404 ENDOD1, BUD13P1
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 AMOTL1, LNCRNA-IUR, 240 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3916760copy number variation1nstd102humanUncertain significance NCBI36 chr11: 93,697,096-95,454,478 , GRCh38 chr11: 94,324,282-96,081,666 , GRCh37 chr11: 94,057,448-95,814,830 SESN3, SRSF8BP, 36 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 LOC101060084, PGAM1P9, 230 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 RPS6P16, CTSC, 449 more genes
    nsv3901353copy number variation1nstd102humanBenign GRCh37 chr11: 94,871,544-94,977,013 , GRCh38.p12 chr11: 95,138,380-95,243,849 LNCRNA-IUR, LOC100129203, 2 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3897292copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057 FAM181B, LOC107984371, 218 more genes
    nsv3894488copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924 RNU6-16P, DDX10, 270 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
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