| | CCDC146, CCDC201 +4735 more | Copy number loss | See cases | |
| | LOC129998995, LOC129998996 +2212 more | Copy number gain | See cases | |
| | LOC129999548, LOC129999549 +1547 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | TMEM139-AS1, TMEM140 +1052 more | Copy number gain | See cases | |
| | MIR5707, MIR595 +1046 more | Copy number gain | See cases | |
| | LOC123956245, LOC123956246 +1025 more | Copy number gain | See cases | |
| | LOC285889, LOC349160 +1025 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129999467, LOC129999468 +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 | |
| | LOC129389950, LOC129999513 +707 more | Copy number loss | See cases | |
| | LOC129389931, LOC129389932 +573 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | TRC-GCA22-1, TRC-GCA23-1 +540 more | Copy number loss | See cases | |
| | LOC129999578, LOC129999579 +538 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129389937, LOC129389938 +526 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126860222, LOC126860223 +329 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129999605, LOC129999606 +205 more | Copy number gain | See cases | |
| | LOC110121278, LOC110121279 +191 more | Copy number loss | See cases | |
| | | 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) | Long QT syndrome 2 +3 more | |
| | | Single nucleotide variant (stop lost) | Cardiovascular phenotype | |
| | | 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 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +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) | Cardiac arrhythmia +2 more | |
| | | Duplication (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +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) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +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) | Cardiac arrhythmia +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) | Cardiac arrhythmia | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +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) | not provided +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 (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |