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Items: 1 to 100 of 3914

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129935413, LOC129935414
+1097 more
Copy number gain
See cases
GPathogenic
AAMP, ABCA12
+1703 more
Copy number gain
See cases
GPathogenic
ABCA12, ABCB6
+1687 more
Copy number gain
See cases
GPathogenic
AAMP, ABCA12
+1665 more
Copy number gain
See cases
GPathogenic
FAM117B, FAM237A
+509 more
Copy number loss
See cases
GPathogenic
LOC126806461, LOC126806467
+1299 more
Copy number gain
See cases
GPathogenic
OR6B3, OTOS
+1148 more
Copy number gain
See cases
GPathogenic
ABCA12, ATIC
+36 more
Copy number gain
See cases
GUncertain significance
ABCA12, BARD1
+10 more
Copy number gain
See cases
GUncertain significance
BARD1
(S264fs +4 more)
Deletion
(frameshift variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GLikely benign
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GBenign
BARD1
Duplication
(3 prime UTR variant +1 more)
not provided
GBenign
BARD1
Duplication
(3 prime UTR variant +1 more)
Familial cancer of breast
+1 more
GBenign/Likely benign
BARD1
Duplication
(3 prime UTR variant +1 more)
not provided
+1 more
GBenign
BARD1
Duplication
(3 prime UTR variant +1 more)
Breast neoplasm
GConflicting classifications of pathogenicity
BARD1
Deletion
(3 prime UTR variant +1 more)
Familial cancer of breast
+1 more
GBenign
BARD1
Deletion
(3 prime UTR variant +1 more)
Familial cancer of breast
GBenign
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
Familial cancer of breast
GBenign
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1, LOC129935540
+1 more
Deletion
Familial cancer of breast
GPathogenic
BARD1, LOC129935540
+3 more
Deletion
Familial cancer of breast
GPathogenic
BARD1
Deletion
Familial cancer of breast
GLikely pathogenic
LOC129935540, LOC129935541
+1 more
Deletion
Familial cancer of breast
GPathogenic
BARD1, LOC129935540
+1 more
Duplication
Familial cancer of breast
GUncertain significance
BARD1, LOC129935540
+3 more
Duplication
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast and/or ovarian cancer
GUncertain significance
BARD1, LOC129935540
+1 more
Duplication
Familial cancer of breast
GUncertain significance
LOC129935540, LOC129935541
+3 more
Duplication
Familial cancer of breast
GUncertain significance
BARD1, LOC129935540
+1 more
Deletion
Familial cancer of breast
GPathogenic
BARD1
Deletion
(splice acceptor variant +1 more)
Malignant tumor of breast
GPathogenic
BARD1, LOC129935540
+1 more
Duplication
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(stop lost +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(stop lost +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(stop lost +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(stop lost +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(S264R +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(S758N +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(S777R +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GLikely benign
BARD1
(D263H +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(D306* +4 more)
Duplication
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(L262fs +4 more)
Deletion
(frameshift variant +1 more)
not specified
+3 more
GUncertain significance
BARD1
(L775H +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GUncertain significance
BARD1
(L775F +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(P774L +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(P304A +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
BARD1
(L773P +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(L322V +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(L773F +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(L259* +4 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
BARD1
(E771D +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BARD1
(E752Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(E771* +4 more)
Duplication
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
GLikely benign
BARD1
(F257C +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
GLikely benign
BARD1
(F257fs +4 more)
Deletion
(frameshift variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
BARD1
(S318F +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(S769C +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
(M768I +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
(M298fs +4 more)
Indel
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely pathogenic
BARD1
(M768T +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(M255* +4 more)
Microsatellite
(nonsense +1 more)
Familial cancer of breast
GPathogenic
BARD1
Single nucleotide variant
(non-coding transcript variant +1 more)
Familial cancer of breast
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
BARD1
(V254fs +4 more)
Microsatellite
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
BARD1
(V254A +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(V316M +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(V767L +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(C253Y +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(C766G +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(D252E +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
GLikely benign
BARD1
(I294fs +4 more)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely pathogenic
BARD1
(D765G +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
BARD1
(D252N +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
GLikely benign
BARD1
(I251M +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(I764T +4 more)
Single nucleotide variant
(missense variant +1 more)
BARD1-related condition
+4 more
GUncertain significance
BARD1
(I251fs +4 more)
Duplication
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(I764V +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
BARD1
(F293Y +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(W249C +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
GUncertain significance
BARD1
(W762* +4 more)
Single nucleotide variant
(nonsense +1 more)
Familial cancer of breast
GLikely pathogenic
BARD1
(W292R +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(W762R +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
BARD1
(S761N +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer
+5 more
GConflicting classifications of pathogenicity
BARD1
(S248G +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
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