| | LOC130059149, LOC130059150 +1738 more | Copy number gain | See cases | |
| | LOC130059197, LOC130059198 +575 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130059618, LOC130059619 +1429 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130059185, LOC130059186 +869 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC126862439, LOC126862440 +1031 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC01572, LOC110120572 +17 more | Copy number loss | See cases | |
| | ZFHX3, ZFHX3-AS1 (K2769T +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ZFHX3, ZFHX3-AS1 (D2745N +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | ZFHX3, ZFHX3-AS1 (V3641I +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ZFHX3-related disorder +1 more | |
| | ZFHX3, ZFHX3-AS1 (P2704L +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ZFHX3, ZFHX3-AS1 (R3614T +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ZFHX3, ZFHX3-AS1 (H3611L +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ZFHX3, ZFHX3-AS1 (H2697Y +1 more) | Single nucleotide variant (missense variant) | ZFHX3-related disorder +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (P3600L +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (N3594K +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | ZFHX3, ZFHX3-AS1 (A2648G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (S2636L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (A2629G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (S2614W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Microsatellite (inframe_insertion) | ZFHX3-related disorder | |
| | | Microsatellite (inframe_insertion) | ZFHX3-related disorder | |
| | | Microsatellite (inframe deletion) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (G2613del +1 more) | Microsatellite (inframe_deletion) | ZFHX3-related disorder | |
| | | Microsatellite (inframe deletion) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (G3527C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Microsatellite (inframe_deletion) | not provided +1 more | |
| | | Deletion (inframe deletion) | ZFHX3-related disorder | |
| | | Deletion (inframe_deletion) | ZFHX3-related disorder +1 more | |
| | | Deletion (inframe_deletion) | ZFHX3-related disorder +1 more | |
| | | Microsatellite (inframe insertion) | ZFHX3-related disorder | |
| | | Microsatellite (inframe insertion) | ZFHX3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (G2613del +1 more) | Microsatellite (inframe_deletion) | ZFHX3-related disorder | |
| | | Insertion (inframe insertion) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (G2603S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication (inframe insertion) | ZFHX3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (S2599G +1 more) | Single nucleotide variant (missense variant) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (G2598del +1 more) | Deletion (inframe_deletion) | ZFHX3-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | ZFHX3-related disorder | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | ZFHX3, ZFHX3-AS1 (G3507R +1 more) | Single nucleotide variant (missense variant) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (V2581E +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (F2576L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (S3486F +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (A2558V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (R2554C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (L2520V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (R2515H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (P2514R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (K2506R +1 more) | Single nucleotide variant (missense variant) | ZFHX3-related disorder +1 more | |
| | ZFHX3, ZFHX3-AS1 (P3414H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (P2494A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | ZFHX3, ZFHX3-AS1 (P2490S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (S3399T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (inframe_deletion) | not provided | |
| | | Deletion (inframe_deletion) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | ZFHX3-related disorder +1 more | |
| | | Microsatellite (inframe insertion) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (G3340D +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (Y2396C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (Q3289R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (T2364S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (P2361L +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | ZFHX3, ZFHX3-AS1 (P2306S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (inframe_deletion) | Neurodevelopmental disorder | |
| | ZFHX3, ZFHX3-AS1 (P3218L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (Q3217H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (P2298L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (P2298Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Microsatellite (inframe insertion) | ZFHX3-related disorder | |
| | | Microsatellite (inframe insertion) | ZFHX3-related disorder | |
| | | Microsatellite (inframe deletion) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (Q2283P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (Q2283L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (P2281L +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ZFHX3, ZFHX3-AS1 (S2263L +1 more) | Single nucleotide variant (missense variant) | ZFHX3-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | ZFHX3-related disorder | |
| | ZFHX3, ZFHX3-AS1 (T3157P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ZFHX3, ZFHX3-AS1 (A3117V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (G3099E +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ZFHX3, ZFHX3-AS1 (R3083W +1 more) | Single nucleotide variant (missense variant) | not specified | |