| | LOC130059149, LOC130059150 +1738 more | Copy number gain | See cases | |
| | LOC130059618, LOC130059619 +1429 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126862439, LOC126862440 +1031 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130059708, LOC130059709 +788 more | Copy number gain | See cases | |
| | LINC01081, LINC01082 +781 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130059691, LOC130059692 +566 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130059603, LOC130059604 +227 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | FOXF1-related condition | |
| | | Single nucleotide variant (5 prime UTR variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Deletion | Idiopathic and/or familial pulmonary arterial hypertension | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_insertion) | Alveolar capillary dysplasia with pulmonary venous misalignment +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Insertion (inframe_insertion) | not provided | |
| | | Microsatellite (inframe_insertion) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Insertion (inframe_insertion) | not provided | |
| | | Deletion (inframe_deletion) | Alveolar capillary dysplasia with pulmonary venous misalignment +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | FOXF1-related condition | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | See cases | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Microsatellite (frameshift variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Duplication (frameshift variant) | Abnormal cardiac atrium morphology | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment +3 more | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related condition | |
| | | Single nucleotide variant (nonsense) | FOXF1-related condition | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Alveolar capillary dysplasia with pulmonary venous misalignment | |
| | | Single nucleotide variant (missense variant) | Pyloric stenosis, infantile hypertrophic, 5 | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | FOXF1-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Alveolar capillary dysplasia with pulmonary venous misalignment | |