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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976539insertion1nstd209human GRCh38 chr11: 114,519,964-114,519,964 , GRCh37.p13 chr11: 114,390,686-114,390,686 NXPE1, NXPE2
    nsv5919370copy number variation1nstd209human GRCh38 chr11: 114,559,681-114,559,745 , GRCh37.p13 chr11: 114,430,403-114,430,467 NXPE2, NXPE1
    nsv5916796copy number variation1nstd209human GRCh38 chr11: 114,526,438-114,526,507 , GRCh37.p13 chr11: 114,397,160-114,397,229 NXPE1, NXPE2
    nsv5702973mobile element insertion2nstd211human GRCh38 chr11: 114,559,912-114,559,912 , GRCh37.p13 chr11: 114,430,634-114,430,634 NXPE1, NXPE2
    nsv5647157insertion1nstd207human GRCh38 chr11: 114,559,896-114,559,896 , GRCh37.p13 chr11: 114,430,618-114,430,618 NXPE1, NXPE2
    nsv5645380insertion1nstd207human GRCh38 chr11: 114,519,967-114,519,967 , GRCh37.p13 chr11: 114,390,689-114,390,689 NXPE1, NXPE2
    nsv5604290copy number variation1nstd207human GRCh38 chr11: 114,536,096-114,536,149 , GRCh37.p13 chr11: 114,406,818-114,406,871 NXPE2, NXPE1
    nsv5594173copy number variation1nstd207human GRCh38 chr11: 114,526,438-114,526,507 , GRCh37.p13 chr11: 114,397,160-114,397,229 NXPE1, NXPE2
    nsv5534172insertion1nstd206human GRCh38 chr11: 114,519,963-114,519,970 , GRCh37.p13 chr11: 114,390,685-114,390,692 NXPE1, NXPE2
    nsv5512134copy number variation1nstd206human GRCh38 chr11: 114,536,095-114,536,150 , GRCh37.p13 chr11: 114,406,817-114,406,872 NXPE1, NXPE2
    nsv5510435copy number variation1nstd206human GRCh38 chr11: 114,559,681-114,559,751 , GRCh37.p13 chr11: 114,430,403-114,430,473 NXPE2, NXPE1
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5505847copy number variation1nstd206human GRCh38 chr11: 114,559,292-114,628,633 , GRCh37.p13 chr11: 114,430,014-114,499,355 NXPE4, NXPE1, 2 more genes
    nsv5504135copy number variation1nstd206human GRCh38 chr11: 114,526,440-114,526,508 , GRCh37.p13 chr11: 114,397,162-114,397,230 NXPE1, NXPE2
    nsv5496119copy number variation1nstd206human GRCh38 chr11: 114,543,676-114,543,810 , GRCh37.p13 chr11: 114,414,398-114,414,532 NXPE2, NXPE1
    nsv5495680copy number variation1nstd206human GRCh38 chr11: 114,531,615-114,535,975 , GRCh37.p13 chr11: 114,402,337-114,406,697 NXPE2, NXPE1
    nsv5422175mobile element insertion1nstd206human GRCh38 chr11: 114,559,912-114,559,963 , GRCh37.p13 chr11: 114,430,634-114,430,685 NXPE1, NXPE2
    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
    nsv5348311translocation1nstd200human GRCh38 chr11: 114,543,676-114,543,676 , GRCh38 chr11: 114,543,810-114,543,810 , GRCh37.p13 chr11: 114,414,398-114,414,398 , GRCh37.p13 chr11: 114,414,532-114,414,532 NXPE2, NXPE1
    nsv5348310translocation1nstd200human GRCh38 chr11: 114,526,440-114,526,440 , GRCh38 chr11: 114,526,508-114,526,508 , GRCh37.p13 chr11: 114,397,230-114,397,230 , GRCh37.p13 chr11: 114,397,162-114,397,162 NXPE1, NXPE2
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