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Items: 1 to 20 of 351

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096727copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,448,428-175,443,602 , GRCh38.p12 chr4: 173,527,277-174,522,451 RANP6, FBXO8, 15 more genes
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7051866inversion1nstd229human GRCh38 chr4: 174,332,713-174,338,594 , GRCh37.p13 chr4: 175,253,864-175,259,745 CEP44
    nsv6757520copy number variation1nstd229human GRCh38 chr4: 174,326,305-174,326,362 , GRCh37.p13 chr4: 175,247,456-175,247,513 CEP44
    nsv6751290copy number variation1nstd229human GRCh38 chr4: 174,261,101-174,321,000 , GRCh37.p13 chr4: 175,182,252-175,242,151 FBXO8, CEP44
    nsv6746333copy number variation1nstd229human GRCh38 chr4: 174,282,470-174,338,910 , GRCh37.p13 chr4: 175,203,621-175,260,061 FBXO8, CEP44
    nsv6744925copy number variation1nstd229human GRCh38 chr4: 174,114,359-174,461,481 , GRCh37.p13 chr4: 175,035,510-175,382,632 FBXO8, LINC02268, 3 more genes
    nsv6744085copy number variation1nstd229human GRCh38 chr4: 174,316,927-174,317,079 , GRCh37.p13 chr4: 175,238,078-175,238,230 CEP44
    nsv6743500copy number variation1nstd229human GRCh38 chr4: 174,317,801-174,319,400 , GRCh37.p13 chr4: 175,238,952-175,240,551 CEP44
    nsv6742303copy number variation1nstd229human GRCh38 chr4: 174,328,401-174,443,300 , GRCh37.p13 chr4: 175,249,552-175,364,451 CEP44, LOC105377547, 1 more genes
    nsv6740692copy number variation1nstd229human GRCh38 chr4: 173,724,041-174,933,391 , GRCh37.p13 chr4: 174,645,192-175,854,542 ADAM29, LOC107986204, 16 more genes
    nsv6739880copy number variation1nstd229human GRCh38 chr4: 174,310,095-174,338,754 , GRCh37.p13 chr4: 175,231,246-175,259,905 CEP44
    nsv6739459copy number variation1nstd229human GRCh38 chr4: 174,290,340-174,310,143 , GRCh37.p13 chr4: 175,211,491-175,231,294 CEP44
    nsv6739273copy number variation1nstd229human GRCh38 chr4: 174,324,783-174,325,231 , GRCh37.p13 chr4: 175,245,934-175,246,382 CEP44
    nsv6738711copy number variation1nstd229human GRCh38 chr4: 174,328,765-174,333,822 , GRCh37.p13 chr4: 175,249,916-175,254,973 CEP44
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6392439copy number variation1nstd223human GRCh38 chr4: 174,286,887-174,287,365 , GRCh37.p13 chr4: 175,208,038-175,208,516 CEP44
    nsv6388812copy number variation1nstd223human GRCh38 chr4: 174,287,974-174,288,542 , GRCh37.p13 chr4: 175,209,125-175,209,693 CEP44
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