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ClinVar: public archive of relationships among sequence variation and human phenotype

Nucleic acids research, 2014-01, Vol.42 (Database issue), p.D980-D985

2014

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HGVS Recommendations for the Description of Sequence Variants: 2016 Update

Human mutation, 2016-06, Vol.37 (6), p.564-569

2016

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ClinVar: improving access to variant interpretations and supporting evidence

Nucleic acids research, 2018-01, Vol.46 (D1), p.D1062-D1067

2018

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ClinVar: public archive of interpretations of clinically relevant variants

Nucleic acids research, 2016-01, Vol.44 (D1), p.D862-D868

2016

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The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency

Nucleic acids research, 2013-01, Vol.41 (Database issue), p.D925-D935

2013

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NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

Nucleic acids research, 2012-01, Vol.40 (Database issue), p.D130

2012

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Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

Nucleic acids research, 2014-01, Vol.42 (D1), p.D873-D878

2014

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Using ClinVar as a Resource to Support Variant Interpretation

Current Protocols in Human Genetics, 2016-04, Vol.89 (1), p.8.16.1-8.16.23

2016

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NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

Nucleic acids research, 2012-01, Vol.40 (D1), p.D130-D135

2012

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NCBI Reference Sequences: current status, policy and new initiatives

Nucleic acids research, 2009-01, Vol.37 (Database issue), p.D32-D36

2009

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NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

Nucleic acids research, 2007-01, Vol.35 (Database issue), p.D61-D65

2007

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Gene: a gene-centered information resource at NCBI

Nucleic acids research, 2015-01, Vol.43 (Database issue), p.D36-D42

2015

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ClinGen — The Clinical Genome Resource

The New England journal of medicine, 2015-06, Vol.372 (23), p.2235-2242

2015

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NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

Nucleic acids research, 2005-01, Vol.33 (Database issue), p.D501-D504

2005

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RefSeq: an update on mammalian reference sequences

Nucleic acids research, 2014-01, Vol.42 (Database issue), p.D756-D763

2014

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Database resources of the National Center for Biotechnology Information

Nucleic acids research, 2009, Vol.37 (Database issue), p.D5-D15

2009

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Human immunodeficiency virus type 1, human protein interaction database at NCBI

Nucleic acids research, 2009-01, Vol.37 (Database issue), p.D417-D422

2009

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Database resources of the National Center for Biotechnology Information

Nucleic acids research, 2008-01, Vol.36 (Database issue), p.D13-D21

2008

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RefSeq and LocusLink: NCBI gene-centered resources

Nucleic acids research, 2001-01, Vol.29 (1), p.137-140

2001

Volltextzugriff (PDF)

Database resources of the National Center for Biotechnology Information

Nucleic acids research, 2007-01, Vol.35 (Database issue), p.D5-D12

2007

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Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

Nucleic acids research, 2014-01, Vol.42 (Database issue), p.D873

2014

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Database resources of the National Center for Biotechnology Information

Nucleic acids research, 2005-01, Vol.33 (Database issue), p.D39-D45

2005

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Database resources of the National Center for Biotechnology Information

Nucleic acids research, 2006-01, Vol.34 (Database issue), p.D173-D180

2006

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Human Variome Project Quality Assessment Criteria for Variation Databases

Human mutation, 2016-06, Vol.37 (6), p.549-558

2016

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ClinVar: public archive of relationships among sequence variation and human phenotype

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

ClinVar: improving access to variant interpretations and supporting evidence

ClinVar: public archive of interpretations of clinically relevant variants

Database resources of the National Center for Biotechnology Information

The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency

NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

Using ClinVar as a Resource to Support Variant Interpretation

NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

NCBI Reference Sequences: current status, policy and new initiatives

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

Gene: a gene-centered information resource at NCBI

ClinGen — The Clinical Genome Resource

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

RefSeq: an update on mammalian reference sequences

Database resources of the National Center for Biotechnology Information

Human immunodeficiency virus type 1, human protein interaction database at NCBI

Database resources of the National Center for Biotechnology Information

RefSeq and LocusLink: NCBI gene-centered resources

Database resources of the National Center for Biotechnology Information

Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Human Variome Project Quality Assessment Criteria for Variation Databases

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