| | LOC130008916, LOC130008917 +4836 more | Copy number gain | See cases | |
| | AGAP2, AGAP2-AS1 +199 more | Copy number loss | See cases | |
| | AGAP2, AGAP2-AS1 +162 more | Copy number loss | See cases | |
| | LOC130008150, MARCHF9 (L10P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130008150, MARCHF9 (R25G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130008150, MARCHF9 (E27K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130008150, MARCHF9 (P30S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130008150, MARCHF9 (G33S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130008150, MARCHF9 (G36S) | 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 (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 provided | |
| | | Duplication | Familial melanoma | |
| | | Duplication | Familial melanoma | |
| | | Copy number loss | not provided | |
| | | Duplication | 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 | |