| | | Copy number gain | See cases | |
| | LOC129935343, LOC129935344 +1703 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129935726, LOC129935727 +1665 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129935713, LOC129935714 +1299 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
| | | Duplication (3 prime UTR variant +1 more) | not provided | |
| | | Duplication (3 prime UTR variant +1 more) | Familial cancer of breast +1 more | |
| | | Duplication (3 prime UTR variant +1 more) | Familial cancer of breast +1 more | |
| | | Duplication (3 prime UTR variant +1 more) | Breast neoplasm | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant +1 more) | Familial cancer of breast +1 more | |
| | | Deletion (3 prime UTR variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | BARD1, LOC129935540 +1 more | Deletion | Familial cancer of breast | |
| | BARD1, LOC129935540 +3 more | Deletion | Familial cancer of breast | |
| | | Deletion | Familial cancer of breast | |
| | BARD1, LOC129935540 +1 more | Deletion | Familial cancer of breast | |
| | BARD1, LOC129935540 +1 more | Duplication | Familial cancer of breast | |
| | BARD1, LOC129935540 +3 more | Duplication | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Breast and/or ovarian cancer | |
| | BARD1, LOC129935540 +1 more | Duplication | Familial cancer of breast | |
| | BARD1, LOC129935540 +3 more | Duplication | Familial cancer of breast | |
| | BARD1, LOC129935540 +1 more | Deletion | Familial cancer of breast | |
| | | Deletion (splice acceptor variant +1 more) | Malignant tumor of breast | |
| | BARD1, LOC129935540 +1 more | Duplication | Familial cancer of breast | |
| | | Single nucleotide variant (stop lost +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (stop lost +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (stop lost +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Duplication (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (nonsense +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Indel (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Microsatellite (nonsense +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Microsatellite (frameshift variant +1 more) | Familial cancer of breast +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Deletion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | BARD1-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (nonsense +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |