| | LOC130065566, LOC130065567 +2522 more | Copy number gain | See cases | |
| | LOC125387319, LOC125387320 +1024 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | ANKRD60, APCDD1L +175 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | FAM210B, LOC130066213 (A6V) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (R19W) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A22P) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A22G) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A40T) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (R49Q) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (A54E) | Single nucleotide variant (missense variant) | not specified | |
| | FAM210B, LOC130066213 (H61R) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | See cases | |
| | | 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 | |