| | CELF2, CELF2-AS1 (K267T +21 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | CELF2-related disorder | |
| | CELF2, CELF2-AS1 (R265L +21 more) | Single nucleotide variant (missense variant) | not provided | |
| | CELF2, CELF2-AS1 (G262S +21 more) | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy 97 | |
| | CELF2, CELF2-AS1 (F198fs +21 more) | Deletion (frameshift variant) | not provided | |
| | CELF2, CELF2-AS1 (P279L +21 more) | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy 97 | |
| | CELF2, CELF2-AS1 (A414T +20 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CELF2-AS1, CELF2 (M132T +20 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | CELF2, CELF2-AS1 (R265C +21 more) | Single nucleotide variant (missense variant) | not provided | GPathogenic/Likely pathogenic |
| | CELF2, CELF2-AS1 (D210fs +21 more) | Deletion (frameshift variant) | Developmental and epileptic encephalopathy 97 | |
| | CELF2, CELF2-AS1 (Y490* +21 more) | Single nucleotide variant (nonsense) | not provided | |
| | | Copy number loss | not provided | |
| | CELF2, CELF2-AS1 (R265H +21 more) | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy 97 | |
| | CELF2, CELF2-AS1 (Y280* +21 more) | Duplication (nonsense) | Developmental and epileptic encephalopathy 97 | |
| | CELF2, CELF2-AS1 (R506G +21 more) | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy 97 | |
| | CELF2, CELF2-AS1 (P520S +21 more) | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy 97 | |