Clinvar - Variation Search

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Classification type

Germline (0)
Somatic (0)

Germline classification

Conflicting classifications (0)
Benign (0)
Likely benign (0)
Uncertain significance (0)
Likely pathogenic (0)
Pathogenic (0)

Types of conflicts

P/LP vs LB/B (0)
P/LP vs VUS (0)
VUS vs LB/B (0)

Molecular consequence

Frameshift (0)
Missense (0)
Nonsense (0)
Splice site (0)
ncRNA (0)
Near gene (0)
UTR (0)

Variation type

Deletion (0)
Duplication (0)
Indel (0)
Insertion (0)
Single nucleotide (0)

Variation size

Short variant (< 50 bps) (0)
Structural variant (>= 50 bps) (0)

Variant length

< 1kb, single gene (0)
> 1kb, single gene (0)
> 1kb, multiple genes (0)

Review status

Practice guideline (0)
Expert panel (0)
Multiple submitters (0)
Single submitter (0)
At least one star (0)
Conflicting classifications (0)

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Variation Genes Type Condition Classification, Review status Variation ID VCV accession rs ID

GRCh37 location GRCh38 location Protein change Molecular consequence Germline date last evaluated Somatic clinical impact date last evaluated Oncogenicity date last evaluated

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