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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894150copy number variation1nstd209human GRCh38 chr4: 73,399,955-73,404,114 , GRCh37.p13 chr4: 74,265,672-74,269,831 ALB
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5840376copy number variation1nstd209human GRCh38 chr4: 73,400,022-73,404,147 , GRCh37.p13 chr4: 74,265,739-74,269,864 ALB
    nsv5680544mobile element insertion1nstd211human GRCh38 chr4: 73,416,857-73,416,857 , GRCh37.p13 chr4: 74,282,574-74,282,574 ALB
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5455523copy number variation1nstd206human GRCh38 chr4: 73,399,955-73,404,115 , GRCh37.p13 chr4: 74,265,672-74,269,832 ALB
    nsv5399487mobile element insertion1nstd206human GRCh38 chr4: 73,416,857-73,416,908 , GRCh37.p13 chr4: 74,282,574-74,282,625 ALB
    nsv5346719translocation1nstd200human GRCh38 chr4: 73,404,115-73,404,115 , GRCh38 chr4: 73,399,955-73,399,955 , GRCh37.p13 chr4: 74,269,832-74,269,832 , GRCh37.p13 chr4: 74,265,672-74,265,672 ALB
    nsv5307116copy number variation1nstd204human GRCh38.p13 chr4: 73,399,955-73,404,115 , GRCh37.p13 chr4: 74,265,672-74,269,832 ALB
    nsv5235855copy number variation1nstd204human GRCh38.p13 chr4: 73,400,501-73,406,400 , GRCh37.p13 chr4: 74,266,218-74,272,117 ALB
    nsv5226934copy number variation1nstd204human GRCh38.p13 chr4: 73,399,922-73,404,147 , GRCh37.p13 chr4: 74,265,639-74,269,864 ALB
    nsv5220443copy number variation1nstd204human GRCh38.p13 chr4: 73,398,201-73,402,700 , GRCh37.p13 chr4: 74,263,918-74,268,417 ALB
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800220copy number variation1nstd200human GRCh37 chr4: 74,265,672-74,269,832 , GRCh38.p12 chr4: 73,399,955-73,404,115 ALB
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
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