Database Commons a catalog of biological databases

Database Commons - ClinVar

ClinVar

Citations: 944

z-index 163.63

Short name ClinVar
Full name variation-phenotype relationships
Description ClinVar aggregates information about genomic variation and its relationship to human health.
URL http://www.ncbi.nlm.nih.gov/clinvar/
Year founded
Last update & version NA    v1.0
Availability Free to all users
University/Institution hosted National Center for Biotechnology Information
Address 8600 Rockville Pike,Bethesda,MD 20894,USA
City Bethesda
Province/State MD
Country/Region United States
Contact name Donna R. Maglott
Contact email maglott@ncbi.nlm.nih.gov
Data type(s)
Major organism(s)
Keyword(s)
  • genomic variation
Publication(s)
  • ClinVar: public archive of interpretations of clinically relevant variants. [PMID: 26582918]

    Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover, Wonhee Jang, Kenneth Katz, Michael Ovetsky, George Riley, Amanjeev Sethi, Ray Tully, Ricardo Villamarin-Salomon, Wendy Rubinstein, Donna R Maglott
    Nucleic acids research 2016:44(D1)
    259 Citations (Google Scholar as of 2017-09-08)

    Abstract: ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) at the National Center for Biotechnology Information (NCBI) is a freely available archive for interpretations of clinical significance of variants for reported conditions. The database includes germline and somatic variants of any size, type or genomic location. Interpretations are submitted by clinical testing laboratories, research laboratories, locus-specific databases, OMIM®, GeneReviews™, UniProt, expert panels and practice guidelines. In NCBI's Variation submission portal, submitters upload batch submissions or use the Submission Wizard for single submissions. Each submitted interpretation is assigned an accession number prefixed with SCV. ClinVar staff review validation reports with data types such as HGVS (Human Genome Variation Society) expressions; however, clinical significance is reported directly from submitters. Interpretations are aggregated by variant-condition combination and assigned an accession number prefixed with RCV. Clinical significance is calculated for the aggregate record, indicating consensus or conflict in the submitted interpretations. ClinVar uses data standards, such as HGVS nomenclature for variants and MedGen identifiers for conditions. The data are available on the web as variant-specific views; the entire data set can be downloaded via ftp. Programmatic access for ClinVar records is available through NCBI's E-utilities. Future development includes providing a variant-centric XML archive and a web page for details of SCV submissions. Published by Oxford University Press on behalf of Nucleic Acids Research 2015. This work is written by (a) US Government employee(s) and is in the public domain in the US.

  • ClinVar: public archive of relationships among sequence variation and human phenotype. [PMID: 24234437]

    Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott
    Nucleic acids research 2014:42(Database issue)
    685 Citations (Google Scholar as of 2017-09-08)

    Abstract: ClinVar (http://www.ncbi.nlm.nih.gov/clinvar/) provides a freely available archive of reports of relationships among medically important variants and phenotypes. ClinVar accessions submissions reporting human variation, interpretations of the relationship of that variation to human health and the evidence supporting each interpretation. The database is tightly coupled with dbSNP and dbVar, which maintain information about the location of variation on human assemblies. ClinVar is also based on the phenotypic descriptions maintained in MedGen (http://www.ncbi.nlm.nih.gov/medgen). Each ClinVar record represents the submitter, the variation and the phenotype, i.e. the unit that is assigned an accession of the format SCV000000000.0. The submitter can update the submission at any time, in which case a new version is assigned. To facilitate evaluation of the medical importance of each variant, ClinVar aggregates submissions with the same variation/phenotype combination, adds value from other NCBI databases, assigns a distinct accession of the format RCV000000000.0 and reports if there are conflicting clinical interpretations. Data in ClinVar are available in multiple formats, including html, download as XML, VCF or tab-delimited subsets. Data from ClinVar are provided as annotation tracks on genomic RefSeqs and are used in tools such as Variation Reporter (http://www.ncbi.nlm.nih.gov/variation/tools/reporter), which reports what is known about variation based on user-supplied locations.

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200 OK2016-04-22
200 OK2016-04-19
200 OK2016-04-15
200 OK2016-04-12
200 OK2016-04-08
200 OK2016-04-05
200 OK2016-04-01
200 OK2016-03-29
200 OK2016-03-28
200 OK2016-03-25
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200 OK2016-03-21
200 OK2016-03-18
200 OK2016-03-16
200 OK2016-03-14
200 OK2016-03-11
200 OK2016-03-09
200 OK2016-03-07
200 OK2016-03-04
200 OK2016-03-02
200 OK2016-02-29
200 OK2016-02-26
200 OK2016-02-24
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200 OK2016-02-19
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200 OK2016-02-15
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200 OK2016-02-08
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200 OK2016-01-29
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Tags

DNA
Homo sapiens
genomic variation

Record metadata

  • Created on: 2015-06-20
  • Curated by:
    • Lina Ma [2017-09-08]
    • Mengwei Li [2016-04-12]
    • Mengwei Li [2016-03-31]
    • Lin Liu [2016-01-29]
    • Lin Liu [2016-01-05]
    • Lina Ma [2015-12-29]
    • Mengwei Li [2015-12-02]
    • Mengwei Li [2015-06-27]
Stats