| | | Duplication | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Duplication (intron variant) | Inborn genetic diseases +3 more | |
| | | Deletion (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Deletion (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Insertion (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Microsatellite (inframe_deletion) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Insertion (frameshift variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Deletion (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F +2 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease dominant intermediate F +1 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease dominant intermediate F | |