| | | 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 | Cataract 46 juvenile-onset | |
| | | Deletion | Schizophrenia | |
| | | Duplication | Schizophrenia | |
| | GPR89B, LOC129931326 +123 more | Deletion | Radial aplasia-thrombocytopenia syndrome | |
| | ANKRD34A, ANKRD35 +55 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | 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 +53 more | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +52 more | Copy number gain | See cases | |
| | | Deletion | Cataract 46 juvenile-onset | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Copy number gain | See cases | |
| | | Variation (no sequence alteration +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Variation (no sequence alteration) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | EBV-positive nodal T- and NK-cell lymphoma | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | not specified | |
| | ANKRD34A, ANKRD35 +15 more | Copy number gain | not provided | |
| | ANKRD34A, ANKRD35 +15 more | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | ANKRD34A, ANKRD35 +18 more | Copy number gain | not provided | |
| | | Copy number gain | Chromosome 1q21.1 duplication syndrome | |
| | ANKRD34A, ANKRD35 +15 more | Copy number gain | Chromosome 1q21.1 deletion syndrome | |