| | PCDHG@, PCDHGA1 +21 more (T490I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (H437Y) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (Q734R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R377P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (V304M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R222H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (T184I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P174S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (N165H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P160L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R141P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R118C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (V106A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (H573D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (N905S +14 more) | Single nucleotide variant (missense variant) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (S818R +14 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | PCDHG@, PCDHGA1 +21 more (E401V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (Q243H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (E672K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (Q800K +14 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +21 more (R809Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R537Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R629H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (L815V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (D724Y) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (S677C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (G11R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P469R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (T767K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (H545R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P297H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R32H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R141C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R377W) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R377Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R73H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (I695T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R323G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R323H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R314H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R883H +14 more) | Single nucleotide variant (missense variant) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R323C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (V385M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (I228M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (G784D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P511S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (M529L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (A615T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P798T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (E572K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (N236S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R118H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (D768E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Duplication | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | PCDHGA10, PCDHGA11 +21 more | Single nucleotide variant (synonymous variant) | not provided | |
| | PCDHGA10, PCDHGA11 +21 more | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number gain | not provided | |
| | C5orf24, C5orf34 +600 more | Deletion | Neurodevelopmental disorder | |
| | | Copy number loss | not provided | |
| | ANKHD1-EIF4EBP3, CHSY3 +385 more | 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 | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129994992, LOC129994993 +1157 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ANKHD1, ANKHD1-DT +377 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |