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Items: 1 to 100 of 14665

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC112533659, LOC112533660
+2032 more
Copy number gain
See cases
GPathogenic
AARSD1, AATF
+1753 more
Copy number gain
See cases
GPathogenic
AARSD1, ACBD4
+633 more
Copy number gain
See cases
GPathogenic
LOC126862571, LOC130060934
+6 more
Deletion
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
LOC126862571, LOC130060934
+6 more
Deletion
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Deletion
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Microsatellite
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Indel
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Indel
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Deletion
Hereditary breast ovarian cancer syndrome
GPathogenic
BRCA1, LOC110485084
+2 more
Deletion
Hereditary breast ovarian cancer syndrome
GPathogenic
BRCA1, LOC126862571
Deletion
Hereditary breast ovarian cancer syndrome
GPathogenic
BRCA1
Deletion
Hereditary breast ovarian cancer syndrome
GPathogenic
BRCA1
Deletion
Hereditary breast ovarian cancer syndrome
GPathogenic
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Microsatellite
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
+1 more
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
+1 more
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Microsatellite
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GLikely benign
BRCA1
Duplication
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GLikely benign
BRCA1
Deletion
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Deletion
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Deletion
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GUncertain significance
BRCA1
Deletion
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Deletion
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GUncertain significance
BRCA1
Deletion
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Deletion
(splice acceptor variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
+2 more
GBenign/Likely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
+1 more
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant)
BRCA1-related disorder
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+1 more
GConflicting classifications of pathogenicity
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Deletion
(splice acceptor variant)
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Indel
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Deletion
Familial cancer of breast
GPathogenic
BRCA1
Deletion
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant)
BRCA1-related disorder
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
+1 more
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
+1 more
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Indel
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant)
Hereditary breast ovarian cancer syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary breast ovarian cancer syndrome
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant)
not provided
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
BRCA1-related disorder
+1 more
GBenign/Likely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
BRCA1
Deletion
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant)
Breast-ovarian cancer, familial, susceptibility to, 1
+1 more
GLikely benign
BRCA1
Deletion
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BRCA1
Deletion
Hereditary breast ovarian cancer syndrome
GPathogenic
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+2 more
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GUncertain significance
BRCA1
Single nucleotide variant
(3 prime UTR variant)
Familial cancer of breast
GLikely benign
BRCA1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 1
GBenign
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