How to construct URLs to display data from ClinVar
Data in ClinVar can be accessed by URLs. The result may be a single record, or a set of records that satisfy the query. These examples are a sample only; any field or property listed in the help documentation can be used to build a URL by combining the base URL with the qualifier.
The base url is:
http://www.ncbi.nlm.nih.gov/clinvar/
which also takes you to ClinVar's home page.
Add the value in the Qualifier column to construct the final URL.
Type | Qualifier | Example |
---|---|---|
Variation accession | /variation/VCV000007105 | http://www.ncbi.nlm.nih.gov/clinvar/variation/VCV000007105 |
Reference accession | RCV000007523 | http://www.ncbi.nlm.nih.gov/clinvar/RCV000007523 |
Submission accession | ?term=SCV000071392[clv_acc] | http://www.ncbi.nlm.nih.gov/clinvar/?term=SCV000071392[clv_acc] |
AlleleID | ?term=22144[alleleid] | http://www.ncbi.nlm.nih.gov/clinvar/?term=22144[alleleid] |
Gene - symbol | ?term=ABCC6[sym] | http://www.ncbi.nlm.nih.gov/clinvar/?term=ABCC6[sym] |
Gene - MIM number | ?term=603234[mim] | http://www.ncbi.nlm.nih.gov/clinvar/?term=603234[mim] |
Gene - GeneID | ?term=672[geneid] | http://www.ncbi.nlm.nih.gov/clinvar/?term=672[geneid] |
Gene - HGNC id |
?term=1884[hgnc] or ?term="HGNC:1884"[hgnc] |
|
GeneReviews NBK accession | ?term=NBK1247 | http://www.ncbi.nlm.nih.gov/clinvar/?term=NBK1247 |
Disease - Name | ?term=noonan | http://www.ncbi.nlm.nih.gov/clinvar/?term=noonan |
Disease - MIM | ?term=264800[mim] | http://www.ncbi.nlm.nih.gov/clinvar/?term=264800[mim] |
Disease - MedGen CUI | ?term=C0033847 | http://ncbi.nlm.nih.gov/clinvar/?term=C0033847 |
Variant - c. expression | ?term=c.1018delG | http://www.ncbi.nlm.nih.gov/clinvar/?term=c.1018delG |
VariationID | variation/7105 | http://www.ncbi.nlm.nih.gov/clinvar/variation/7105 |
Interpretation (a property) |
?term="clinsig pathogenic"[Properties] | http://www.ncbi.nlm.nih.gov/clinvar?term=%22clinsig%20pathogenic%22[Properties] |
Combination of Interpretation and review status (both properties) |
?term="clinsig pathogenic"[Properties] AND "revstat expert panel"[Properties] | http://www.ncbi.nlm.nih.gov/clinvar?term=%22clinsig%20pathogenic%22[Properties]%20AND%20%22revstat%20expert%20panel%22[Properties] |
Chromosome position [as a range delimited by a colon (:)] Use [chrpos37] for GRCh37/hg19 and [chrpos38] for GRCh38/hg38 Use [chrpos] for the current assembly |
?term=17[chr] AND 43000000:44000000[chrpos37] | http://www.ncbi.nlm.nih.gov/clinvar/?term=17[chr]+AND+43000000:44000000[chrpos37] |