| | 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 | |
| | LOC129999653, LOC129999654 +1380 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129999666, LOC129999667 +1052 more | Copy number gain | See cases | |
| | TMEM140, TMEM176A +1046 more | Copy number gain | See cases | |
| | LOC129999503, LOC129999504 +1025 more | Copy number gain | See cases | |
| | LINC00996, LINC01003 +1025 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | WDR86, WDR86-AS1 +944 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | AGBL3, CYREN (T170A +2 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | AGBL3, CYREN (D232A +2 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | AGBL3, CYREN (P285L +2 more) | Single nucleotide variant (missense variant +4 more) | not provided | |
| | AGBL3, CYREN (A799V +2 more) | Single nucleotide variant (missense variant +4 more) | not specified | |
| | AGBL3, CYREN (I308N +3 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | AGBL3, CYREN (Y108* +3 more) | Single nucleotide variant (missense variant +4 more) | not specified | |
| | AGBL3, CYREN (P324S +2 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | AGBL3, CYREN (G308A +2 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | AGBL3, CYREN (N339H +2 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | AGBL3, CYREN (E901K +2 more) | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Copy number loss | not specified | |
| | | Deletion | not provided | |
| | | 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 gain | not provided | |
| | | Copy number loss | Small face +7 more | |
| | | Copy number loss | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Complex | Renal transitional cell carcinoma | |
| | | Copy number gain | not provided | |
| | | Copy number loss | 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 | |