| | LOC121740684, LOC121740685 +4735 more | Copy number loss | See cases | |
| | LOC111674474, LOC111674475 +2212 more | Copy number gain | See cases | |
| | LOC129999548, LOC129999549 +1547 more | Copy number gain | See cases | |
| | LOC129999373, LOC129999374 +492 more | Copy number loss | See cases | |
| | LOC129999653, LOC129999654 +1380 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129999356, LOC129999357 +284 more | Copy number loss | See cases | |
| | | 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 | |
| | | 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 | |
| | | 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 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | GCC1, LOC126860171 (R415K) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (L410P) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (L401V) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (E381Q) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (Q357E) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (M342V) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (L320V) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (A279T) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (R278Q) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (R272P) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (H234R) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (R210C) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (A204V) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (T174I) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (D155N) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (G145R) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (P127L) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (P126S) | Single nucleotide variant (missense variant) | not specified | |
| | GCC1, LOC126860171 (T108N) | 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 | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | See cases | |
| | CACNA2D1, CADPS2 +896 more | Complex | Ring chromosome 7 | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Deletion | Pleomorphic xanthoastrocytoma | |
| | | Copy number loss | See cases | |