| | LOC126860963, LOC126860964 +1008 more | Copy number gain | See cases | |
| | LOC129390190, LOC129390191 +610 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC130004132, LOC130004133 +150 more | Copy number loss | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (5 prime UTR variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (5 prime UTR variant) | Dilated cardiomyopathy 1W | |
| | | Deletion | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W +1 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated Cardiomyopathy, Dominant +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W +1 more | |
| | | Inversion (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Deletion (splice donor variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Deletion (intron variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Duplication (intron variant) | Dilated cardiomyopathy 1W | |
| | | Deletion (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Indel (intron variant) | Cardiomyopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1W +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1W | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1W | |