| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC123477714, LOC123477715 +1267 more | Copy number gain | Neurodevelopmental disorder | |
| | LOC129992145, LOC129992146 +1209 more | Copy number gain | See cases | |
| | LOC129992028, LOC129992029 +691 more | Copy number loss | See cases | |
| | LOC126806993, LOC126806994 +702 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129992237, LOC129992238 +861 more | Copy number gain | See cases | |
| | LOC129992157, LOC129992158 +832 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129992561, LOC129992562 +1409 more | Copy number gain | Neurodevelopmental disorder | |
| | LOC129992261, LOC129992262 +962 more | Copy number gain | Neurodevelopmental disorder | |
| | FGFBP1, LOC126806998 +393 more | Copy number loss | 4p partial monosomy syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | KCNIP4, LOC105374511 +13 more | Copy number loss | See cases | |
| | LOC105374511, LOC126806996 +1 more | Copy number gain | See cases | |
Click to view in NCBI Gene