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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4685758copy number variation1nstd102humanPathogenic GRCh37 chr6: 1,307,929-1,856,280 , GRCh38.p12 chr6: 1,307,694-1,856,046 LOC105374883, FOXF2-DT, 12 more genes

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    Related information

    • ClinVar
      Clinical reports for this variation
    • Functional Class
      Functional class of the sequence domain architecture
    • Gene
      Link from dbVar to Gene
    • OMIM
      Link from dbVar to OMIM
    • Pathways + GO
      Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
    • PubMed
      Link from dbVar to PubMed
    • Taxonomy
      Link from dbVar to Taxonomy

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