| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease X-linked dominant 6 | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease X-linked dominant 6 | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Duplication (5 prime UTR variant) | not provided | |
| | | Duplication (intron variant) | Charcot-Marie-Tooth disease X-linked dominant 6 | |
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