| | | 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 | |
| | LOC101928343, CD300E (R168Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101928343, CD300E (V160M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CD300E, LOC101928343 (N150K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101928343, CD300E (V127I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101928343, CD300E (R51L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CD300E, LOC101928343 (C50R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CD300E, LOC101928343 (A28V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CD300E, LOC101928343 (L16F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | 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 | |