| | LOC130005128, LOC130005129 +723 more | Copy number gain | See cases | |
| | LOC130005114, LOC130005115 +204 more | Copy number gain | See cases | |
| | LOC111718490, LOC112067719 +388 more | Copy number gain | See cases | |
| | LOC130005104, LOC130005105 +271 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Duplication | Small for gestational age | |
| | | Copy number loss | Autism spectrum disorder | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | Beckwith-Wiedemann syndrome due to 11p15 microdeletion | |
| | C11orf42, MRGPRG +210 more | Copy number gain | Russell-Silver syndrome | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Duplication | Immunodeficiency 39 | |
| | | Copy number gain | not provided | |
| | | Duplication | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |