| | | Copy number loss | See cases | |
| | LOC129389795, LOC129389796 +636 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Duplication | Autism | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (P29L) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (Y31C) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (A35P) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (A37E) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (L38V) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (S41F) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (A44V) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (V50A) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (T55P) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (G60S) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (H64Y) | Single nucleotide variant (missense variant) | not specified | |
| | LANCL2, LOC129998459 (H64Q) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | 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 gain | not provided | |
| | | Copy number loss | See cases | |
| | CACNA2D1, CADPS2 +896 more | Complex | Ring chromosome 7 | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Deletion | Pleomorphic xanthoastrocytoma | |
| | | Copy number loss | See cases | |
| | | Inversion | Childhood apraxia of speech | |