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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963301insertion1nstd209human GRCh38 chr8: 58,441,351-58,441,351 , GRCh37.p13 chr8: 59,353,910-59,353,910 UBXN2B
    nsv5694906mobile element insertion1nstd211human GRCh38 chr8: 58,445,613-58,445,613 , GRCh37.p13 chr8: 59,358,172-59,358,172 UBXN2B
    nsv5478180copy number variation1nstd206human GRCh38 chr8: 58,432,858-58,433,190 , GRCh37.p13 chr8: 59,345,417-59,345,749 UBXN2B
    nsv5407184mobile element insertion1nstd206human GRCh38 chr8: 58,445,613-58,445,664 , GRCh37.p13 chr8: 59,358,172-59,358,223 UBXN2B
    nsv5342231translocation1nstd200human GRCh37 chr8: 59,349,833-59,349,833 , GRCh37 chr8: 59,349,763-59,349,763 , GRCh38.p12 chr8: 58,437,274-58,437,274 , GRCh38.p12 chr8: 58,437,204-58,437,204 UBXN2B
    nsv5113114mobile element insertion1nstd203human GRCh38 chr8: 58,446,779-58,446,815 , GRCh37.p13 chr8: 59,359,338-59,359,374 UBXN2B
    nsv4965363copy number variation1nstd200human GRCh38 chr8: 58,402,015-58,459,588 , GRCh37.p13 chr8: 59,314,574-59,372,147 UBXN2B, PTPN11P2
    nsv4960455copy number variation1nstd200human GRCh38 chr8: 58,437,204-58,437,274 , GRCh37.p13 chr8: 59,349,763-59,349,833 UBXN2B
    nsv4960454copy number variation1nstd200human GRCh38 chr8: 58,432,594-58,462,611 , GRCh37.p13 chr8: 59,345,153-59,375,170 UBXN2B
    nsv4813250copy number variation1nstd200human GRCh37 chr8: 59,345,153-59,375,170 , GRCh38.p12 chr8: 58,432,594-58,462,611 UBXN2B
    nsv4604818copy number variation1nstd183human GRCh37 chr8: 59,342,950-59,345,921 , GRCh38.p12 chr8: 58,430,391-58,433,362 UBXN2B
    nsv4555637insertion1nstd166human GRCh37.p13 chr8: 59,355,947-59,355,947 , GRCh38.p12 chr8: 58,443,388-58,443,388 UBXN2B
    nsv4541652insertion1nstd166human GRCh37.p13 chr8: 59,353,918-59,353,918 , GRCh38.p12 chr8: 58,441,359-58,441,359 UBXN2B
    nsv4490523mobile element insertion1nstd166human GRCh37.p13 chr8: 59,358,158-59,358,158 , GRCh38.p12 chr8: 58,445,599-58,445,599 UBXN2B
    nsv4478515mobile element insertion1nstd166human GRCh37.p13 chr8: 59,357,509-59,357,509 , GRCh38.p12 chr8: 58,444,950-58,444,950 UBXN2B
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4341038sequence alteration1nstd166human GRCh37.p13 chr8: 59,345,438-59,345,439 , GRCh38.p12 chr8: 58,432,879-58,432,880 UBXN2B
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
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