| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129931352, LOC129931353 +183 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC126805854, LOC128071544 +179 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126805853, LOC126805854 +153 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +73 more | Copy number loss | 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 | See cases | |
| | | Copy number loss | See cases | |
| | LOC101927468, LOC106783502 +143 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129931329, LOC129931330 +143 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | MIR5087, MIR6077 +143 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | GPathogenic/Likely pathogenic |
| | | Copy number gain | See cases | |
| | LOC101927468, LOC106783502 +133 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +67 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | RNVU1-6, RNVU1-7 +118 more | Deletion | Schizophrenia | |
| | LOC129931347, LOC129931348 +104 more | Deletion | Schizophrenia | |
| | ANKRD34A, ANKRD35 +66 more | Copy number gain | See cases | GConflicting classifications of pathogenicity |
| | | Copy number loss | See cases | |
| | | Deletion | Schizophrenia | |
| | | Duplication | Schizophrenia | |
| | LOC129931348, LOC129931349 +52 more | Duplication | Schizophrenia | |
| | ANKRD34A, ANKRD35 +52 more | Deletion | Schizophrenia | |
| | ANKRD34A, ANKRD35 +52 more | Duplication | Schizophrenia | |
| | GPR89B, LOC129931326 +123 more | Deletion | Radial aplasia-thrombocytopenia syndrome | |
| | ANKRD34A, ANKRD35 +43 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +55 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +54 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +52 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +44 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +52 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +43 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +54 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +50 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +42 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +42 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +42 more | Copy number gain | See cases | Gconflicting data from submitters |
| | ANKRD34A, ANKRD35 +41 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +50 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +35 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +41 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +41 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +50 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +49 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +53 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +52 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +40 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +47 more | Copy number loss | Radial aplasia-thrombocytopenia syndrome | |
| | LOC129931331, NUDT17 (A2T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931331, NUDT17 (A2G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931331, NUDT17 (L8R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931331, NUDT17 (S22C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931331, NUDT17 (S22T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931331, NUDT17 (G34R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931331, NUDT17 (T35P) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931332, NUDT17 (P81L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931332, NUDT17 (V91A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931332, NUDT17 (R113P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129931332, NUDT17 (V117G) | 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 | |
| | ANKRD34A, ANKRD35 +14 more | Copy number loss | not provided | |