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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923590copy number variation1nstd209human GRCh38 chr11: 83,256,823-83,268,098 , GRCh37.p13 chr11: 82,967,865-82,979,140 CCDC90B
    nsv5917359copy number variation1nstd209human GRCh38 chr11: 83,270,505-83,271,301 , GRCh37.p13 chr11: 82,981,547-82,982,343 CCDC90B
    nsv5847598copy number variation1nstd209human GRCh38 chr11: 83,256,814-83,268,134 , GRCh37.p13 chr11: 82,967,856-82,979,176 CCDC90B
    nsv5696004mobile element insertion1nstd211human GRCh38 chr11: 83,283,675-83,283,675 , GRCh37.p13 chr11: 82,994,718-82,994,718 CCDC90B
    nsv5498423copy number variation1nstd206human GRCh38 chr11: 83,269,377-83,271,656 , GRCh37.p13 chr11: 82,980,419-82,982,698 CCDC90B
    nsv5399965mobile element insertion1nstd206human GRCh38 chr11: 83,283,675-83,283,722 , GRCh37.p13 chr11: 82,994,718-82,994,765 CCDC90B
    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
    nsv5184709mobile element insertion1nstd203human GRCh38 chr11: 83,276,715-83,276,729 , GRCh37.p13 chr11: 82,987,758-82,987,772 CCDC90B
    nsv4987599copy number variation1nstd200human GRCh38 chr11: 83,254,458-83,273,248 , GRCh37.p13 chr11: 82,965,500-82,984,291 CCDC90B, ANKRD42
    nsv4987598copy number variation1nstd200human GRCh38 chr11: 83,237,179-83,261,558 , GRCh37.p13 chr11: 82,948,221-82,972,600 ANKRD42, CCDC90B
    nsv4835471copy number variation1nstd200human GRCh37 chr11: 82,948,221-82,972,600 , GRCh38.p12 chr11: 83,237,179-83,261,558 ANKRD42, CCDC90B
    nsv4729116copy number variation1nstd102humanUncertain significance GRCh37 chr11: 82,618,269-83,454,773 , GRCh38.p12 chr11: 82,907,227-83,743,730 RAB30, RAB30-DT, 18 more genes
    nsv4616350copy number variation2nstd183human GRCh37 chr11: 82,984,698-82,985,634 , GRCh38.p12 chr11: 83,273,655-83,274,591 CCDC90B
    nsv4612332copy number variation1nstd183human GRCh37 chr11: 82,984,757-82,985,101 , GRCh38.p12 chr11: 83,273,714-83,274,058 CCDC90B
    nsv4611109copy number variation1nstd183human GRCh37 chr11: 82,985,058-82,985,228 , GRCh38.p12 chr11: 83,274,015-83,274,185 CCDC90B
    nsv4206421copy number variation1nstd166human GRCh37.p13 chr11: 82,980,546-82,982,698 , GRCh38.p12 chr11: 83,269,504-83,271,656 CCDC90B
    nsv4198122copy number variation1nstd166human GRCh37.p13 chr11: 82,966,000-82,984,000 , GRCh38.p12 chr11: 83,254,958-83,272,958 ANKRD42, CCDC90B
    nsv4196246copy number variation1nstd166human GRCh37.p13 chr11: 82,948,221-82,972,600 , GRCh38.p12 chr11: 83,237,179-83,261,558 CCDC90B, ANKRD42
    nsv3924587copy number variation1nstd102humanUncertain significance GRCh37 chr11: 82,777,166-84,186,433 , NCBI36 chr11: 82,454,814-83,864,081 , GRCh38 chr11: 83,066,124-84,475,390 RAB30, ANKRD42-DT, 17 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
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