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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962993insertion1nstd209human GRCh38 chr6: 112,241,152-112,241,152 , GRCh37.p13 chr6|NW_003871062.1: 238,673-238,673 , GRCh37.p13 chr6: 112,562,353-112,562,353 LAMA4-AS1, LAMA4
    nsv5888036copy number variation1nstd209human GRCh38 chr6: 112,109,644-112,109,806 , GRCh37.p13 chr6|NW_003871062.1: 107,166-107,328 , GRCh37.p13 chr6: 112,430,847-112,431,009 LAMA4
    nsv5717551mobile element insertion1nstd211human GRCh38 chr6: 112,138,174-112,138,174 , GRCh37.p13 chr6|NW_003871062.1: 135,695-135,695 , GRCh37.p13 chr6: 112,459,376-112,459,376 LOC107986633, LAMA4
    nsv5693924mobile element insertion2nstd211human GRCh38 chr6: 112,116,665-112,116,665 , GRCh37.p13 chr6|NW_003871062.1: 114,187-114,187 , GRCh37.p13 chr6: 112,437,868-112,437,868 LAMA4, LOC107986633
    nsv5682589mobile element insertion2nstd211human GRCh38 chr6: 112,221,694-112,221,694 , GRCh37.p13 chr6|NW_003871062.1: 219,215-219,215 , GRCh37.p13 chr6: 112,542,895-112,542,895 LAMA4
    nsv5681244mobile element insertion1nstd211human GRCh38 chr6: 112,160,874-112,160,874 , GRCh37.p13 chr6|NW_003871062.1: 158,395-158,395 , GRCh37.p13 chr6: 112,482,076-112,482,076 LAMA4
    nsv5675900mobile element insertion1nstd211human GRCh38 chr6: 112,157,082-112,157,082 , GRCh37.p13 chr6|NW_003871062.1: 154,603-154,603 , GRCh37.p13 chr6: 112,478,284-112,478,284 LAMA4
    nsv5639355insertion1nstd207human GRCh38 chr6: 112,241,152-112,241,152 , GRCh37.p13 chr6|NW_003871062.1: 238,673-238,673 , GRCh37.p13 chr6: 112,562,353-112,562,353 LAMA4-AS1, LAMA4
    nsv5631518insertion1nstd207human GRCh38 chr6: 112,210,865-112,210,865 , GRCh37.p13 chr6|NW_003871062.1: 208,386-208,386 , GRCh37.p13 chr6: 112,532,066-112,532,066 LAMA4
    nsv5629325insertion1nstd207human GRCh38 chr6: 112,221,680-112,221,680 , GRCh37.p13 chr6: 112,542,881-112,542,881 , GRCh37.p13 chr6|NW_003871062.1: 219,201-219,201 LAMA4
    nsv5564719copy number variation1nstd207human GRCh38 chr6: 112,109,644-112,109,806 , GRCh37.p13 chr6: 112,430,847-112,431,009 , GRCh37.p13 chr6|NW_003871062.1: 107,166-107,328 LAMA4
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5560054mobile element insertion1nstd206human GRCh38 chr6: 112,138,174-112,138,225 , GRCh37.p13 chr6|NW_003871062.1: 135,695-135,746 , GRCh37.p13 chr6: 112,459,376-112,459,427 LAMA4, LOC107986633
    nsv5459080copy number variation1nstd206human GRCh38 chr6: 112,109,646-112,109,807 , GRCh37.p13 chr6|NW_003871062.1: 107,168-107,329 , GRCh37.p13 chr6: 112,430,849-112,431,010 LAMA4
    nsv5402692mobile element insertion1nstd206human GRCh38 chr6: 112,157,082-112,157,133 , GRCh37.p13 chr6|NW_003871062.1: 154,603-154,654 , GRCh37.p13 chr6: 112,478,284-112,478,335 LAMA4
    nsv5402218mobile element insertion1nstd206human GRCh38 chr6: 112,116,665-112,116,716 , GRCh37.p13 chr6|NW_003871062.1: 114,187-114,238 , GRCh37.p13 chr6: 112,437,868-112,437,919 LAMA4, LOC107986633
    nsv5400885mobile element insertion1nstd206human GRCh38 chr6: 112,221,694-112,221,745 , GRCh37.p13 chr6|NW_003871062.1: 219,215-219,266 , GRCh37.p13 chr6: 112,542,895-112,542,946 LAMA4
    nsv5396773mobile element insertion1nstd206human GRCh38 chr6: 112,160,874-112,160,925 , GRCh37.p13 chr6|NW_003871062.1: 158,395-158,446 , GRCh37.p13 chr6: 112,482,076-112,482,127 LAMA4
    nsv5388619copy number variation2nstd186human GRCh37 chr6: 112,430,849-112,431,010 , GRCh38.p12 chr6: 112,109,646-112,109,807 LAMA4
    nsv5369619translocation1nstd200human GRCh38 chr6: 112,119,930-112,119,930 , GRCh38 chr6: 112,121,284-112,121,284 , GRCh37.p13 chr6: 112,442,487-112,442,487 , GRCh37.p13 chr6|NW_003871062.1: 117,452-117,452 , GRCh37.p13 chr6|NW_003871062.1: 118,806-118,806 , GRCh37.p13 chr6: 112,441,133-112,441,133 LAMA4, LOC107986633
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