| | LOC130066574, LOC130066575 +1159 more | Copy number gain | See cases | |
| | LOC130066796, LOC130066797 +1160 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066513, LOC130066514 +1160 more | Copy number gain | See cases | |
| | LOC126653326, LOC126653327 +1160 more | Copy number gain | See cases | |
| | LOC130066833, LOC130066834 +1160 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066700, LOC130066701 +1159 more | Copy number gain | See cases | |
| | LOC130066665, LOC130066666 +1160 more | Copy number gain | See cases | |
| | ADAMTS1, ADAMTS5 +643 more | Copy number loss | See cases | |
| | LOC126653316, LOC126653317 +1160 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066758, LOC130066759 +1159 more | Copy number gain | See cases | |
| | LOC130066436, LOC130066437 +1159 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | KRTAP13-3, KRTAP13-4 +1157 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066541, LOC130066542 +1159 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066593, LOC130066594 +1155 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066830, LOC130066831 +1155 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129391220, LOC129391221 +1156 more | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Microsatellite (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (no sequence alteration) | Congenital long QT syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Duplication (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Deletion (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Deletion (3 prime UTR variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Jervell and Lange-Nielsen syndrome 2 +3 more | GConflicting classifications of pathogenicity |
| | | Duplication | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +3 more | |
| | | Deletion (3 prime UTR variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 5 +3 more | GConflicting classifications of pathogenicity |
| | | Duplication | not specified | |
| | | Single nucleotide variant (stop lost) | Long QT syndrome | |
| | | Deletion (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |