| | LOC130005128, LOC130005129 +723 more | Copy number gain | See cases | |
| | LOC130005123, LOC130005124 +204 more | Copy number gain | See cases | |
| | LOC106799843, LOC106865369 +388 more | Copy number gain | See cases | |
| | LOC106783508, LOC106799843 +271 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | A-GAMMA3'E, ABCC8 +917 more | Copy number gain | See cases | |
| | BGLT3, A-GAMMA3'E +328 more | Deletion | Thalassemia, gamma-delta-beta | |
| | | Copy number loss | See cases | |
| | KRTAP5-6, KRTAP5-AS1 +129 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (synonymous variant +2 more) | H19-related condition | |
| | HOTS, MRPL23 +1 more (L81F) | Single nucleotide variant (missense variant +2 more) | H19-related condition | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | H19-related condition | |
| | | Single nucleotide variant (synonymous variant +2 more) | H19-related condition | |
| | | Microsatellite (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | H19-related condition | |
| | | Single nucleotide variant (missense variant +2 more) | H19-related condition | |
| | HOTS, MRPL23 +1 more (T38M) | Single nucleotide variant (missense variant +2 more) | H19-related condition | |
| | | Single nucleotide variant (missense variant +2 more) | H19-related condition | |
| | | Single nucleotide variant (missense variant +2 more) | H19-related condition | |
| | | Single nucleotide variant (intron variant) | H19-related condition | |
| | | Deletion (intron variant) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | MIR675-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Copy number gain | See cases | |
| | | Deletion | Wilms tumor 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Beckwith-Wiedemann syndrome | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | Beckwith-Wiedemann syndrome | |
| | | Single nucleotide variant (genic upstream transcript variant) | Beckwith-Wiedemann syndrome | |
| | | Copy number gain | Wilms tumor 2 | |
| | | Single nucleotide variant (intron variant) | H19-related condition | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | Beckwith-Wiedemann syndrome | |
| | | Single nucleotide variant (intron variant) | H19-related condition | |
| | | Single nucleotide variant (genic upstream transcript variant) | Beckwith-Wiedemann syndrome | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | H19-related condition | |
| | | Single nucleotide variant | Beckwith-Wiedemann syndrome | |
| | | Single nucleotide variant (intron variant) | H19-related condition | |
| | | Single nucleotide variant (intron variant) | H19-related condition | |
| | | Copy number gain | not provided | |
| | C11orf42, MRGPRG +210 more | Copy number gain | Russell-Silver syndrome | |
| | | Duplication | Autosomal recessive DOPA responsive dystonia | |
| | | Duplication | not provided | |
| | | Duplication | Neuronal ceroid lipofuscinosis | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Beckwith-Wiedemann syndrome | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Duplication | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Duplication | Immunodeficiency 39 +1 more | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number gain | not provided | |
| | | Duplication | Neuronal ceroid lipofuscinosis | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | CHORDC1, CHRDL2 +1293 more | Copy number gain | not provided | |
| | AAMDC, AASDHPPT +1292 more | 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 | |
| | AAMDC, AASDHPPT +1289 more | 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 | |