| | ADAM19, ADAMTS2 +1166 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995246, LOC129995247 +622 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995359, LOC129995360 +386 more | Copy number loss | See cases | |
| | FAM153A, FAM153B +176 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129995374, LOC129995375 +136 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ARL10, NOP16 (K174Q +2 more) | Single nucleotide variant (synonymous variant +3 more) | not specified | |
| | ARL10, NOP16 (L170V +1 more) | Single nucleotide variant (synonymous variant +4 more) | not specified | |
| | ARL10, NOP16 (S169Y +4 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | ARL10, NOP16 (R144W +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ARL10, NOP16 (Q142E +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ARL10, NOP16 (D131G +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ARL10, NOP16 (R130H +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ARL10, NOP16 (W99* +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ARL10, NOP16 (R115H +3 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARL10, NOP16 (K106N +3 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARL10, NOP16 (L81P +2 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ARL10, LOC126807615 +1 more (R69L +2 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARL10, LOC126807615 +1 more (R45W +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Deletion | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Hunter-McAlpine craniosynostosis | |
| | | Copy number gain | not provided | |
| | | Copy number gain | 5q35 microduplication syndrome | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | Sotos syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |