| | | Copy number gain | See cases | |
| | LOC130067011, LOC130067012 +535 more | Copy number gain | See cases | |
| | LOC126863153, LOC126863154 +2088 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +798 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC130067137, LOC130067138 +823 more | Copy number gain | See cases | |
| | | 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 | |
| | | Duplication | Schizophrenia | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |
| | IGLV4-3, LINC01659 +163 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +160 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +160 more | Copy number gain | See cases | GConflicting classifications of pathogenicity |
| | ADORA2A, ADORA2A-AS1 +162 more | Copy number gain | See cases | |
| | LOC130067089, LOC130067090 +160 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +157 more | Copy number gain | See cases | |
| | LOC130067070, LOC130067071 +124 more | Copy number gain | See cases | |
| | LOC130067246, LOC130067247 +556 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +84 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +81 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +81 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +80 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +80 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +80 more | Copy number gain | See cases | |
| | | Duplication | Schizophrenia | |
| | | Duplication | Schizophrenia | |
| | LOC130067107, LOC130067108 +74 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +76 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +76 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +70 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +76 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +74 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +74 more | Copy number gain | See cases | GConflicting classifications of pathogenicity |
| | ADORA2A, ADORA2A-AS1 +74 more | Copy number gain | See cases | |
| | DERL3, LOC111721701 +3 more | Duplication | Intellectual disability, autosomal dominant 15 | |
| | DERL3, LOC111721701 +5 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +57 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Chromosome 22q11.2 microduplication syndrome | |
| | | Duplication | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Unilateral renal agenesis | |
| | | Copy number gain | Chromosome 22q11.2 microduplication syndrome | |
| | | Deletion | Agammaglobulinemia 2, autosomal recessive | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Generalized-onset seizure +1 more | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Duplication | Epilepsy +1 more | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Cat eye syndrome +1 more | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Deletion | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | not provided | |