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ClinVar

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Result Filters

Classification type
Clear
- Germline (0)
- Somatic (0)

Germline classification
Clear
- Conflicting classifications (0)
- Benign (0)
- Likely benign (0)
- Uncertain significance (0)
- Likely pathogenic (0)
- Pathogenic (0)

Types of conflicts
Clear
- P/LP vs LB/B (0)
- P/LP vs VUS (0)
- VUS vs LB/B (0)

Molecular consequence
Clear
- Frameshift (0)
- Missense (0)
- Nonsense (0)
- Splice site (0)
- ncRNA (0)
- Near gene (0)
- UTR (0)

Variation type
Clear
- Deletion (0)
- Duplication (0)
- Indel (0)
- Insertion (0)
- Single nucleotide (0)

Variation size
Clear
- Short variant (< 50 bps) (0)
- Structural variant (>= 50 bps) (0)

Variant length
Clear
- < 1kb, single gene (0)
- > 1kb, single gene (0)
- > 1kb, multiple genes (0)

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

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Classification type
Germline classification
Types of conflicts
Molecular consequence
Variation type
Variation size
Variant length
Review status
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The following term was not found in ClinVar: 86223540[HGNC].
No items found.

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