| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | A3GALT2, ACOT11 +1226 more | Inversion | Bilateral polymicrogyria | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | C1orf210, C1orf50 +91 more | Copy number loss | Epilepsy syndrome | |
Click to view in NCBI Gene