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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970795inversion1nstd209human GRCh38 chr9: 114,106,457-114,343,345 , GRCh37.p13 chr9: 116,868,737-117,105,625 ORM1, ORM2, 5 more genes
    nsv5923990copy number variation1nstd209human GRCh38 chr9: 114,325,971-114,332,658 , GRCh37.p13 chr9: 117,088,251-117,094,938 ORM1, ORM2, 1 more genes
    nsv5916614copy number variation1nstd209human GRCh38 chr9: 114,319,730-114,321,100 , GRCh37.p13 chr9: 117,082,010-117,083,380 ORM1
    nsv5914544copy number variation1nstd209human GRCh38 chr9: 114,324,738-114,331,514 , GRCh37.p13 chr9: 117,087,018-117,093,794 ORM2, ORM1
    nsv5911636copy number variation1nstd209human GRCh38 chr9: 114,320,569-114,321,417 , GRCh37.p13 chr9: 117,082,849-117,083,697 ORM1
    nsv5864005copy number variation7nstd209human GRCh38 chr9: 114,322,597-114,329,463 , GRCh37.p13 chr9: 117,084,877-117,091,743 ORM1, ORM2
    nsv5856694copy number variation2nstd209human GRCh38 chr9: 114,319,746-114,321,145 , GRCh37.p13 chr9: 117,082,026-117,083,425 ORM1
    nsv5853741copy number variation7nstd209human GRCh38 chr9: 114,323,272-114,326,069 , GRCh37.p13 chr9: 117,085,552-117,088,349 ORM1
    nsv5853414copy number variation6nstd209human GRCh38 chr9: 114,322,598-114,326,543 , GRCh37.p13 chr9: 117,084,878-117,088,823 ORM1
    nsv5852494copy number variation5nstd209human GRCh38 chr9: 114,325,163-114,331,210 , GRCh37.p13 chr9: 117,087,443-117,093,490 ORM2, ORM1
    nsv5851833copy number variation7nstd209human GRCh38 chr9: 114,324,038-114,326,069 , GRCh37.p13 chr9: 117,086,318-117,088,349 ORM1
    nsv5849276copy number variation1nstd209human GRCh38 chr9: 114,321,046-114,323,674 , GRCh37.p13 chr9: 117,083,326-117,085,954 ORM1
    nsv5644496insertion1nstd207human GRCh38 chr9: 114,322,709-114,322,709 , GRCh37.p13 chr9: 117,084,989-117,084,989 ORM1
    nsv5634332insertion1nstd207human GRCh38 chr9: 114,324,829-114,324,829 , GRCh37.p13 chr9: 117,087,109-117,087,109 ORM1
    nsv5594862copy number variation1nstd207human GRCh38 chr9: 114,319,730-114,321,100 , GRCh37.p13 chr9: 117,082,010-117,083,380 ORM1
    nsv5485127copy number variation1nstd206human GRCh38 chr9: 114,319,732-114,321,101 , GRCh37.p13 chr9: 117,082,012-117,083,381 ORM1
    nsv5479187copy number variation1nstd206human GRCh38 chr9: 114,320,703-114,321,450 , GRCh37.p13 chr9: 117,082,983-117,083,730 ORM1
    nsv5418166copy number variation1nstd206human GRCh38 chr9: 114,326,414-114,334,552 , GRCh37.p13 chr9: 117,088,694-117,096,832 ORM1, ORM2, 1 more genes
    nsv5381739copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,956,664-117,267,081 , GRCh38.p12 chr9: 114,194,384-114,504,801 COL27A1, ORM1, 6 more genes
    nsv5315003copy number variation1nstd204human GRCh38.p13 chr9: 114,319,732-114,321,101 , GRCh37.p13 chr9: 117,082,012-117,083,381 ORM1
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