| | LINC02522, LINC02525 +823 more | Copy number gain | See cases | |
| | LOC132089500, LOC132090749 +641 more | Copy number gain | See cases | |
| | LOC129995714, LOC129995715 +777 more | Copy number gain | See cases | |
| | LOC129995520, LOC129995521 +610 more | Copy number loss | See cases | |
| | LOC121106426, LOC121113497 +557 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC02521, LINC02522 +508 more | Copy number gain | See cases | |
| | BLOC1S5, BLOC1S5-TXNDC5 +435 more | Copy number gain | See cases | |
| | LOC129995778, LOC129995779 +571 more | Copy number gain | See cases | |
| | LOC126859546, LOC126859547 +431 more | Copy number loss | See cases | |
| | LOC129995630, LOC129995631 +536 more | Copy number gain | See cases | |
| | LOC129389446, LOC129389447 +617 more | Copy number loss | See cases | |
| | LOC129995913, LOC129995914 +1340 more | Copy number gain | See cases | |
| | | 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 | Woolly hair-skin fragility syndrome +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 | Lethal acantholytic epidermolysis bullosa +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 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) | Cardiomyopathy +1 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) | Lethal acantholytic epidermolysis bullosa +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | | 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) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | 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) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +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) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | DSP-related condition | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +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 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +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 right ventricular dysplasia 8 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +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) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +4 more | GConflicting classifications of pathogenicity |
| | | 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) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +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) | Cardiovascular phenotype +9 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +4 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (nonsense) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 8 +1 more | |