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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5932030copy number variation1nstd209human GRCh38 chr12: 120,568,665-120,569,726 , GRCh37.p13 chr12: 121,006,468-121,007,529 RNF10
    nsv5931516copy number variation1nstd209human GRCh38 chr12: 120,545,482-120,555,336 , GRCh37.p13 chr12: 120,983,285-120,993,139 RNF10
    nsv5929830copy number variation1nstd209human GRCh38 chr12: 120,555,276-120,555,896 , GRCh37.p13 chr12: 120,993,079-120,993,699 RNF10
    nsv5864050copy number variation1nstd209human GRCh38 chr12: 120,544,729-120,546,978 , GRCh37.p13 chr12: 120,982,532-120,984,781 RNF10
    nsv5862587copy number variation1nstd209human GRCh38 chr12: 120,547,279-120,548,378 , GRCh37.p13 chr12: 120,985,082-120,986,181 RNF10
    nsv5862135copy number variation1nstd209human GRCh38 chr12: 120,560,494-120,561,493 , GRCh37.p13 chr12: 120,998,297-120,999,296 RNF10
    nsv5861421copy number variation1nstd209human GRCh38 chr12: 120,552,279-120,555,276 , GRCh37.p13 chr12: 120,990,082-120,993,079 RNF10
    nsv5859372copy number variation2nstd209human GRCh38 chr12: 120,550,679-120,551,978 , GRCh37.p13 chr12: 120,988,482-120,989,781 RNF10
    nsv5852236copy number variation1nstd209human GRCh38 chr12: 120,546,479-120,548,578 , GRCh37.p13 chr12: 120,984,282-120,986,381 RNF10
    nsv5850191copy number variation1nstd209human GRCh38 chr12: 120,545,979-120,549,678 , GRCh37.p13 chr12: 120,983,782-120,987,481 RNF10
    nsv5849009copy number variation2nstd209human GRCh38 chr12: 120,554,477-120,555,476 , GRCh37.p13 chr12: 120,992,280-120,993,279 RNF10
    nsv5847739copy number variation1nstd209human GRCh38 chr12: 120,568,694-120,569,693 , GRCh37.p13 chr12: 121,006,497-121,007,496 RNF10
    nsv5700924mobile element insertion2nstd211human GRCh38 chr12: 120,561,112-120,561,112 , GRCh37.p13 chr12: 120,998,915-120,998,915 RNF10
    nsv5655782insertion1nstd207human GRCh38 chr12: 120,561,098-120,561,098 , GRCh37.p13 chr12: 120,998,901-120,998,901 RNF10
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv5495074copy number variation1nstd206human GRCh38 chr12: 120,568,640-120,569,699 , GRCh37.p13 chr12: 121,006,443-121,007,502 RNF10
    nsv5416006mobile element insertion1nstd206human GRCh38 chr12: 120,561,112-120,561,163 , GRCh37.p13 chr12: 120,998,915-120,998,966 RNF10
    nsv5378965translocation1nstd200human GRCh38 chr8: 4,441,118-4,441,118 , GRCh38 chr12: 120,553,034-120,553,034 , GRCh37.p13 chr12: 120,990,837-120,990,837 , GRCh37.p13 chr8: 4,298,640-4,298,640 RNF10, CSMD1
    nsv5377701translocation1nstd200human GRCh38 chr4: 151,322,432-151,322,432 , GRCh38 chr12: 120,553,031-120,553,031 , GRCh37.p13 chr4: 152,243,584-152,243,584 , GRCh37.p13 chr12: 120,990,834-120,990,834 RNF10, SH3D19
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