| | LOC129929105, LOC129929106 +2149 more | Copy number gain | Trisomy 12p | |
| | ATAD3C, AURKAIP1 +520 more | Copy number loss | See cases | |
| | LOC129929144, LOC129929145 +458 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LINC01786, LINC02593 +338 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129929188, LOC129929189 +332 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | TMEM201, TMEM240 +806 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129929181, LOC129929182 +401 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129929093, LOC129929094 +274 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129929186, LOC129929187 +577 more | Copy number loss | See cases | |
| | LOC121677383, LOC121967042 +277 more | Copy number loss | See cases | |
| | LOC132088688, LOC132088689 +264 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | ACTRT2, ARHGEF16 +117 more | Copy number gain | See cases | |
| | LOC126805582, LOC126805583 +88 more | Copy number gain | Anomalous pulmonary venous return | |
| | ACTRT2, LOC112577578 +13 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | ACTRT2, LOC110120751 +15 more | Copy number gain | See cases | Gconflicting data from submitters |
| | ACTRT2, LOC112577578 +13 more | Copy number gain | See cases | |
| | ACTRT2, LOC105378604 +20 more | Copy number loss | See cases | |
| | LOC112577578, LOC124903827 +13 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC112577578, LOC112577579 +199 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ACTRT2, LOC124903827 +8 more | Copy number gain | See cases | |
| | AADACL3, AADACL4 +804 more | Copy number loss | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Microsatellite | not provided | |
| | | Duplication | Left ventricular noncompaction 8 | |
| | LOC105378604, LOC110120751 +14 more | Deletion | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | PRDM16, LOC124903827 (R2Q) | Single nucleotide variant (missense variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Deletion (intron variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (intron variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (intron variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (intron variant) | Left ventricular noncompaction 8 +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Deletion (inframe_deletion) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (missense variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (missense variant) | PRDM16-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (missense variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (missense variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (synonymous variant) | Left ventricular noncompaction 8 | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Left ventricular noncompaction 8 +1 more | |