| | | Copy number gain | See cases | |
| | LOC120908923, LOC120947224 +1352 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129932855, LOC129932856 +1168 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC02765, LINC02768 +955 more | Copy number gain | See cases | |
| | LOC440742, LYPD8 +955 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129932825, LOC129932826 +952 more | Copy number gain | See cases | |
| | LOC129932658, LOC129932659 +950 more | Copy number gain | See cases | |
| | LOC126806053, LOC126806054 +870 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 | |
| | | Deletion | Autism | |
| | DISC1, DISC2 +1 more (D484H +3 more) | Single nucleotide variant (non-coding transcript variant +3 more) | not specified | |
| | TSNAX-DISC1, DISC1 +1 more (L607F +2 more) | Single nucleotide variant (non-coding transcript variant +4 more) | not provided | |
| | DISC1, DISC2 +1 more (S504N +2 more) | Single nucleotide variant (non-coding transcript variant +3 more) | not specified | |
| | DISC1, DISC2 +1 more (L649P +2 more) | Single nucleotide variant (non-coding transcript variant +3 more) | not specified | |
| | DISC1, DISC2 +1 more (A537V +2 more) | Single nucleotide variant (non-coding transcript variant +3 more) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +3 more) | DISC1-related disorder | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | | Duplication | Actin accumulation myopathy | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Duplication | Parathyroid carcinoma +2 more | |
| | | Copy number gain | See cases | |
| | C1orf35, C1orf74 +320 more | Copy number gain | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | 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 | |
| | GPATCH2, GPATCH3 +2014 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | AVPR1B, B3GALNT2 +393 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |