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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398044copy number variation1nstd102humanPathogenic NCBI36 chr21: 13,636,378-28,138,533 , GRCh37 chr21: 14,714,507-29,216,662 , GRCh38.p12 chr21: 13,342,186-27,844,343 LONRF2P5, RHOT1P2, 171 more genes

    Supplemental Content

    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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