| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ARB2A, ARRDC3-AS1 +146 more | Copy number loss | See cases | |
| | LOC129994229, LOC129994230 +688 more | Copy number loss | See cases | |
| | LOC129994369, LOC129994370 +495 more | Copy number loss | See cases | |
| | LOC129994289, LOC129994290 +342 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | 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 | |
| | GPR150, LOC129994226 (L125R) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (L128P) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (R148W) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (P160S) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (R162H) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (A163D) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (L164R) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (G168D) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC129994226 (A176T) | 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 | |
| | GPR150, LOC129994227 (V231G) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (A269T) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (R288H) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (G332S) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (M342I) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (R361Q) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (L370R) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (G371C) | Single nucleotide variant (missense variant) | not specified | |
| | GPR150, LOC123497940 (E384Q) | 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 | See cases | |
| | | Copy number loss | not specified | |
| | | Deletion | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not specified | |
| | | Copy number gain | See cases | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | ADAMTS19, ADGRV1 +104 more | Copy number gain | not provided | |
| | C5orf24, C5orf34 +600 more | Deletion | Neurodevelopmental disorder | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Deletion | Hereditary cancer-predisposing syndrome +1 more | |
| | | 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 | |