| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | PRKAB2, RNVU1-27 +168 more | Copy number gain | See cases | |
| | LOC129931323, LOC129931324 +153 more | 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 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 | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | 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 | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | GPathogenic/Likely pathogenic |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ANKRD34A, ANKRD35 +61 more | Copy number loss | See cases | |
| | ANKRD34A, ANKRD35 +67 more | Copy number loss | See cases | |
| | LOC129931346, LOC129931347 +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 +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 | |
| | LOC129931345, LOC129931346 +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 | |
| | | Copy number loss | 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 +50 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 +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 +47 more | Copy number loss | Radial aplasia-thrombocytopenia syndrome | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (3 prime UTR variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (synonymous variant) | 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 (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hemochromatosis type 2A | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hemochromatosis type 2A | |
| | | 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 (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 (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | 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 (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |