| | LINC02811, LITATS1 +1147 more | Copy number gain | See cases | |
| | A3GALT2, ACOT11 +1226 more | Inversion | Bilateral polymicrogyria | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | SCMH1, SLFNL1-AS1 (R654Q +12 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (E510G +12 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (R408Q +12 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (R412L +12 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (E398D +12 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (D464G +12 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | SCMH1, SLFNL1-AS1 (S380N +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (C486Y +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (P481L +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (M342V +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (R501C +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | SCMH1, SLFNL1-AS1 (G399V +7 more) | 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 +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not specified | |
| | | Deletion | Severe combined immunodeficiency due to CTPS1 deficiency | |
| | | Copy number gain | Intellectual disability, mild +1 more | |
| | | Duplication | Charcot-Marie-Tooth disease dominant intermediate C | |
| | | Copy number gain | See cases | |
| | GPATCH2, GPATCH3 +2014 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |