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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970069insertion1nstd209human GRCh38 chr11: 108,180,542-108,180,542 , GRCh37.p13 chr11: 108,051,269-108,051,269 NPAT
    nsv5921371copy number variation1nstd209human GRCh38 chr11: 108,209,329-108,217,463 , GRCh37.p13 chr11: 108,080,056-108,088,190 NPAT
    nsv5920917copy number variation1nstd209human GRCh38 chr11: 108,165,884-108,166,033 , GRCh37.p13 chr11: 108,036,611-108,036,760 NPAT
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5853932copy number variation1nstd209human GRCh38 chr11: 108,209,997-108,217,118 , GRCh37.p13 chr11: 108,080,724-108,087,845 NPAT
    nsv5708359mobile element insertion2nstd211human GRCh38 chr11: 108,180,557-108,180,557 , GRCh37.p13 chr11: 108,051,284-108,051,284 NPAT
    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
    nsv5672617copy number variation1nstd102humanPathogenic GRCh37 chr11: 108,093,770-108,114,855 , GRCh38.p12 chr11: 108,223,043-108,244,128 NPAT, ATM
    nsv5672616copy number variation1nstd102humanPathogenic GRCh37 chr11: 108,093,770-108,100,060 , GRCh38.p12 chr11: 108,223,043-108,229,333 NPAT, ATM
    nsv5549199insertion1nstd206human GRCh38 chr11: 108,187,705-108,187,736 , GRCh37.p13 chr11: 108,058,432-108,058,463 NPAT
    nsv5534333insertion1nstd206human GRCh38 chr11: 108,180,557-108,180,577 , GRCh37.p13 chr11: 108,051,284-108,051,304 NPAT
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5506767copy number variation1nstd206human GRCh38 chr11: 108,217,945-108,218,202 , GRCh37.p13 chr11: 108,088,672-108,088,929 NPAT
    nsv5499148copy number variation1nstd206human GRCh38 chr11: 108,209,319-108,217,464 , GRCh37.p13 chr11: 108,080,046-108,088,191 NPAT
    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
    nsv5361517translocation1nstd200human GRCh38 chr11: 108,178,573-108,178,573 , GRCh38 chr11: 108,178,494-108,178,494 , GRCh37.p13 chr11: 108,049,221-108,049,221 , GRCh37.p13 chr11: 108,049,300-108,049,300 NPAT
    nsv5134571mobile element insertion1nstd203human GRCh38 chr11: 108,180,542-108,180,557 , GRCh37.p13 chr11: 108,051,269-108,051,284 NPAT
    nsv5130103mobile element insertion1nstd203human GRCh38 chr11: 108,180,539-108,180,557 , GRCh37.p13 chr11: 108,051,266-108,051,284 NPAT
    nsv5124555mobile element insertion1nstd203human GRCh38 chr11: 108,178,695-108,178,700 , GRCh37.p13 chr11: 108,049,422-108,049,427 NPAT
    nsv4989273copy number variation1nstd200human GRCh38 chr11: 107,591,412-108,213,389 , GRCh37.p13 chr11: 107,462,138-108,084,116 , NPAT, 9 more genes
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