{
  "package" : "hl7.terminology.r5@6.3.0",
  "definition" : "dbVar-Germline",
  "system" : "http://terminology.hl7.org/CodeSystem/v2-0396",
  "property" : [ {
    "_uri" : "http://terminology.hl7.org/CodeSystem/utg-concept-properties#v2-concComment",
    "code" : "v2-concComment",
    "valueString" : "dbVar is NCBI's database of genomic structural variations (including copy number variants) that are larger than 50 contiguous base pairs. It is the complement of dbSNP, which only contains variants occurring in 50 or fewer contiguous base pairs.   It contains insertions, deletions, duplications, inversions, multi-nucleotide substitutions, mobile element insertions, translocations, and complex chromosomal rearrangements."
  }, {
    "_uri" : "http://terminology.hl7.org/CodeSystem/utg-concept-properties#status",
    "code" : "status",
    "valueCode" : "A"
  } ],
  "codesystem" : "cb8cdb18-a074-5e6c-a3b7-57416f28931c",
  "concept_id" : "46a1d9b5-e06a-592c-9203-daf0ea797a19",
  "ancestors" : {
    "dbVar-GL" : 0
  },
  "id" : "a3b8ce2b-bdfc-42c0-8739-f71fcb58cd05",
  "code" : "dbVar-GL",
  "display" : "dbVar-Germline",
  "version" : "4.1.0"
}