| | | Copy number loss | See cases | |
| | LOC129932075, LOC129932076 +560 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | ANGPTL1, APOBEC4 +455 more | Copy number loss | See cases | |
| | LOC129388668, LOC129388669 +477 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | C1orf21, C1orf21-DT +37 more | Copy number loss | See cases | |
| | C1orf21, C1orf21-DT +46 more | Copy number loss | See cases | |
| | GS1-204I12.4, HMCN1 +44 more | Copy number loss | See cases | |
| | | Deletion (frameshift variant) | Immunodeficiency 70 | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | Immunodeficiency 70 | |
| | | Single nucleotide variant (missense variant) | IVNS1ABP-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | IVNS1ABP-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | Immunodeficiency 70 | |
| | | Single nucleotide variant (missense variant) | IVNS1ABP-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Immunodeficiency 70 | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | IVNS1ABP-related disorder | |
| | | Duplication (intron variant) | IVNS1ABP-related disorder | |
| | | Single nucleotide variant (intron variant) | IVNS1ABP-related disorder | |
| | | Single nucleotide variant (synonymous variant) | IVNS1ABP-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not provided | |
| | | Duplication | Gastrointestinal stromal tumor +2 more | |
| | | Deletion | Immunodeficiency 70 | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |