| | MIR636, MIR6516 +1033 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC130061806, SYNGR2 (A9T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061806, SYNGR2 (A9G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061806, SYNGR2 (A30T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061806, SYNGR2 (A30S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130061808, SYNGR2 (R242W +1 more) | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Duplication | Idiopathic generalized epilepsy | |
| | ANAPC11, ARHGDIA +146 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ALOX12, ALOX12B +1143 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |