Skip to content
GET /v1/meta

Endpoint catalogue & notes

Try it live

10 free calls per day — no sign-up, no API key. Goes through the oanor gateway.

Custom headers (optional)
api.oanor.com/dbvar-api

It works. Grab an API key and use it in your project.

Get an API key

Code snippets

curl "https://api.oanor.com/dbvar-api/v1/meta" \
  -H "x-oanor-key: oanor_test_..."
await fetch("https://api.oanor.com/dbvar-api/v1/meta", {
  headers: { "x-oanor-key": "oanor_test_..." }
});
$ch = curl_init("https://api.oanor.com/dbvar-api/v1/meta");
curl_setopt($ch, CURLOPT_HTTPHEADER, ["x-oanor-key: oanor_test_..."]);
curl_setopt($ch, CURLOPT_RETURNTRANSFER, true);
$out = curl_exec($ch);
import requests
requests.get(
    "https://api.oanor.com/dbvar-api/v1/meta",
    headers={"x-oanor-key": "oanor_test_..."}
)

Example response

A real response from this endpoint, captured by the latest health check.

{
    "data": {
        "note": "dbVar is NCBI's archive of human genomic structural variation — structural variants (SVs) larger than ~50 bp: copy-number variants (CNVs), large deletions and duplications, insertions, inversions and translocations. /v1/search?gene=BRCA1 finds structural variants overlapping a gene (or use q= for free-text), returning each variant's dbVar accession (e.g. nsv7897183), the study it came from, variant type, organism, overlapping genes, GRCh38 genomic placement and clinical significance; /v1/variant?id=nsv7897183 returns a single variant's full record — placements on all assemblies (GRCh37 and GRCh38), variant type, genes, clinical significance, study type, methods and variant counts (you may also pass the numeric uid). Accessions look like nsv… (variant), nssv… (variant call) or nstd… (study). Data from NCBI dbVar (public domain). A structural-variation / CNV resource — distinct from clinical single-nucleotide variant interpretation (ClinVar), population allele frequencies (gnomAD) and trait associations (GWAS). Ideal for genomics, cytogenetics, rare-disease and bioinformatics tools.",
        "source": "NCBI dbVar — database of genomic structural variation (ncbi.nlm.nih.gov/dbvar)",
        "endpoints": [
            "/v1/search",
            "/v1/variant",
            "/v1/meta"
        ]
    },
    "meta": {
        "timestamp": "2026-06-01T23:41:01.124Z",
        "request_id": "91116d99-5379-4d8e-94db-373ca2ae4cb1"
    },
    "status": "ok",
    "message": "Meta retrieved",
    "success": true
}