| | | Copy number gain | 20q13.13qter duplication | |
| | FAM210B, LOC130066213 (A22G) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A22P) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (H61R) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (R19W) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A54E) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A40T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130066213, FAM210B (R49Q) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A6V) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
| | | Deletion | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130066240, LOC130066241 +553 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC130065884, LOC130065885 +2522 more | Copy number gain | See cases | |
| | LOC121627913, LOC121853014 +175 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |