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Items: 1 to 100 of 1142

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(stop lost +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(stop lost +1 more)
Familial cancer of breast
+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)
not specified
+2 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+2 more
GLikely benign
BARD1
(L262fs +4 more)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+3 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
(L773P +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)
Familial cancer of breast
+1 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+2 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
BARD1
(V254fs +4 more)
Microsatellite
(frameshift variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
BARD1
(V767L +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GConflicting classifications of pathogenicity
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
(missense variant +1 more)
Familial cancer of breast
+1 more
GConflicting classifications of pathogenicity
BARD1
(I764T +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
BARD1
(F293Y +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
(S761N +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+5 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
BARD1
(S760L +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(S760W +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(P246I +4 more)
Indel
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(P759A +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(P759S +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
BARD1
(K757N +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
BARD1
(W286C +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
Deletion
(nonsense +1 more)
Familial cancer of breast
+1 more
GPathogenic/Likely pathogenic
BARD1
(W286* +4 more)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
BARD1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
BARD1
(R751Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Breast and/or ovarian cancer
+3 more
GUncertain significance
BARD1
(R751W +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary breast ovarian cancer syndrome
+3 more
GUncertain significance
BARD1
(V750D +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(V750I +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
BARD1
(R749S +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)
Familial cancer of breast
+2 more
GLikely benign
BARD1
(E748G +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(P277T +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)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BARD1
(Y745D +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
BARD1
(N744D +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
(N293* +4 more)
Duplication
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
BARD1
(L742F +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
BARD1
(L742M +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
BARD1
(D741G +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(Y739C +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
(I738V +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GBenign/Likely benign
BARD1
(I224T +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(I737V +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GUncertain significance
BARD1
(Y736C +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(Y736F +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
BARD1
(Q735K +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
+2 more
GLikely benign
BARD1
(T734I +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(T734A +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
(F732L +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
BARD1
(F732C +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GUncertain significance
BARD1
(F732S +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(R731H +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
BARD1
(R731C +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
BARD1
(R731G +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GConflicting classifications of pathogenicity
BARD1
(Q730P +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(Q730E +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(non-coding transcript variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(S728F +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(D727E +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
BARD1
(D727G +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+1 more
GUncertain significance
BARD1
(D727N +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+2 more
GLikely benign
BARD1
(P726S +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(R706K +4 more)
Indel
(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
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GBenign/Likely benign
BARD1
(A724V +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BARD1
(H272D +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BARD1
(Y722N +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+2 more
GLikely benign
BARD1
(A208V +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(A721S +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
(A721T +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+3 more
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(T719A +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
BARD1
(N718S +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+2 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
BARD1
(T716I +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(T716A +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+3 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
BARD1-related disorder
+4 more
GLikely benign
BARD1
(Q715* +4 more)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
BARD1
(V713A +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BARD1
(V713G +4 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
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