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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv516847copy number variation2nstd21human NCBI35 chr3: 66,510,972-66,520,646 , GRCh37.p13 chr3: 66,428,282-66,437,956 , GRCh38.p12 chr3: 66,377,858-66,387,532 , GRCh38.p12 chr3|NW_012132916.1: 354,754-364,428 LRIG1, SLC25A26

    Supplemental Content

    Related information

    • dbGaP
      Link from dbVar to dbGaP
    • Functional Class
      Functional class of the sequence domain architecture
    • Gene
      Link from dbVar to Gene
    • GEO DataSets
      Link from dbVar to GEO DataSets
    • Nucleotide
      Link from dbVar to Nucleotide
    • 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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