| | LOC121740684, LOC121740685 +4735 more | Copy number loss | See cases | |
| | LOC111674474, LOC111674475 +2212 more | Copy number gain | See cases | |
| | LOC129999548, LOC129999549 +1547 more | Copy number gain | See cases | |
| | LOC129999653, LOC129999654 +1380 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129999666, LOC129999667 +1052 more | Copy number gain | See cases | |
| | TMEM140, TMEM176A +1046 more | Copy number gain | See cases | |
| | LOC129999503, LOC129999504 +1025 more | Copy number gain | See cases | |
| | LINC00996, LINC01003 +1025 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | WDR86, WDR86-AS1 +944 more | Copy number loss | See cases | |
| | LOC129999526, LOC129999527 +908 more | Copy number gain | See cases | |
| | | Copy number gain | Neurodevelopmental disorder | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Neurodevelopmental disorder | |
| | LOC129999649, LOC129999650 +737 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129999755, LOC129999756 +573 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC105375556, LOC105375589 +540 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126860247, LOC126860248 +526 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129999582, LOC129999583 +407 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129999632, LOC129999633 +375 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Long QT syndrome | |
| | KCNH2, LOC110121275 +3 more | Deletion | Long QT syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 2 | |
| | KCNH2, LOC110121275 +3 more | Duplication | Long QT syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (stop lost) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Duplication (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 2 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Microsatellite (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiac arrhythmia | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Deletion (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |