| | | 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 (missense variant +1 more) | not specified | |
| | | Copy number loss | not provided | |
| | | 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 (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 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | 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 | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | Gconflicting data from submitters |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | Gconflicting data from submitters |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | GConflicting classifications of pathogenicity |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | KHDRBS2, LOC121740654 +2 more | Copy number gain | See cases | Gconflicting data from submitters |
| | ADGRB3, ADGRB3-DT +105 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | KHDRBS2, LINC00680 +16 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | KHDRBS2, LINC00680 +16 more | Copy number gain | See cases | |
| | KHDRBS2, LOC121740654 +2 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |