| | ADGRB3, ADGRB3-DT +310 more | Copy number loss | See cases | |
| | B3GAT2, LINC00472 +18 more | Copy number gain | See cases | |
| | B3GAT2, LINC00472 +18 more | Copy number gain | See cases | |
| | LOC129996705, OGFRL1 (S27L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129996705, OGFRL1 (E28K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129996705, OGFRL1 (E48G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129996705, OGFRL1 (P53T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129996705, OGFRL1 (P65A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129996705, OGFRL1 (D68E) | 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 (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 loss | Autism | |
| | | Copy number loss | Chromosome 6q11-q14 deletion syndrome | |
| | | Copy number gain | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |