| | | Copy number gain | See cases | |
| | LOC130061805, LOC130061806 +1033 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | GConflicting classifications of pathogenicity |
| | | Copy number gain | See cases | |
| | | Copy number gain | 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 (synonymous variant) | not provided | |
| | CD300LD, CD300LD-AS1 (M94V) | Single nucleotide variant (missense variant) | not specified | |
| | CD300LD, CD300LD-AS1 (D57N) | Single nucleotide variant (missense variant) | not specified | |
| | CD300LD, CD300LD-AS1 (A56T) | Single nucleotide variant (missense variant) | not specified | |
| | CD300LD, CD300LD-AS1 (G33S) | Single nucleotide variant (missense variant) | not specified | |
| | CD300LD, CD300LD-AS1 +1 more | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | TNFSF12, TNFSF12-TNFSF13 +1143 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |