| | | Copy number gain | See cases | |
| | LOC129995555, LOC129995556 +641 more | Copy number gain | See cases | |
| | LOC129995829, LOC129995830 +777 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129995745, LOC129995746 +557 more | Copy number gain | See cases | |
| | LOC110121220, LOC110121246 +2579 more | Copy number gain | See cases | |
| | LOC132090751, LOC132090752 +508 more | Copy number gain | See cases | |
| | LOC132089486, LOC132089487 +435 more | Copy number gain | See cases | |
| | SERPINB9-AS1, SLC22A23 +571 more | Copy number gain | See cases | |
| | BLOC1S5, BLOC1S5-TXNDC5 +431 more | Copy number loss | See cases | |
| | LOC126859578, LOC126859579 +536 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995677, LOC129995678 +331 more | Copy number loss | See cases | |
| | BLOC1S5, BLOC1S5-TXNDC5 +159 more | Copy number loss | See cases | |
| | | Single nucleotide variant (non-coding transcript variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant) | not provided | |
| | | Single nucleotide variant | Arrhythmogenic right ventricular cardiomyopathy +3 more | |
| | | Single nucleotide variant | Lethal acantholytic epidermolysis bullosa +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Lethal acantholytic epidermolysis bullosa +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Epidermolysis bullosa simplex due to plakophilin deficiency +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Arrhythmogenic right ventricular cardiomyopathy +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Lethal acantholytic epidermolysis bullosa +5 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Arrhythmogenic right ventricular dysplasia 8 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Arrhythmogenic right ventricular dysplasia 8 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Arrhythmogenic right ventricular dysplasia 8 +5 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | Epidermolysis bullosa simplex due to plakophilin deficiency +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Deletion | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiomyopathy | |
| | | Deletion | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiomyopathy | |
| | | Indel (5 prime UTR variant) | Cardiovascular phenotype | |
| | | Duplication | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 8 +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +3 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | DSP-related disorder | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Deletion (frameshift variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | not provided | |