| | LOC130055392, LOC130055393 +780 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126861920, LOC126861921 +3280 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130055370, LOC130055371 +840 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Duplication (frameshift variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (splice acceptor variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Dilated cardiomyopathy 1EE +4 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (nonsense) | Hypertrophic cardiomyopathy 14 +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Atrial septal defect 3 +6 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | MYH6-related condition | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (splice acceptor variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | Sick sinus syndrome 3, susceptibility to +5 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (synonymous variant) | MYH6-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +5 more | |
| | | Single nucleotide variant (missense variant) | Atrial septal defect 3 +6 more | |
| | | Single nucleotide variant (synonymous variant) | MYH6-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | MYH6-related condition +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | Cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 14 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy | |