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Items: 1 to 100 of 7466

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCG5, ABCG8
+1631 more
Copy number gain
See cases
GPathogenic
LOC126806252, LOC126806253
+2457 more
Copy number gain
See cases
GBenign
ABCG5, ABCG8
+443 more
Copy number gain
See cases
GPathogenic
LOC129933708, LOC129933709
+104 more
Copy number gain
See cases
GUncertain significance
BCYRN1, CALM2
+53 more
Copy number gain
See cases
GLikely benign
BCYRN1, CALM2
+94 more
Copy number loss
See cases
GPathogenic
BCYRN1, CALM2
+60 more
Copy number gain
See cases
GLikely pathogenic
BCYRN1, EPCAM
+21 more
Copy number gain
See cases
GUncertain significance
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, KCNK12
+19 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
EPCAM, LOC129933695
+2 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
LOC129933695, MIR559
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
LOC129933695, MIR559
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+2 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+1 more
Duplication
Hereditary nonpolyposis colorectal neoplasms
GUncertain significance
EPCAM, LOC129933695
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
EPCAM, LOC129933695
+1 more
Deletion
Hereditary nonpolyposis colorectal neoplasms
GPathogenic
LOC129933695, MSH2
Deletion
Lynch syndrome
GPathogenic
LOC129933695, MSH2
Deletion
Lynch syndrome
GPathogenic
LOC129933695, MSH2
Deletion
(genic upstream transcript variant)
Hereditary cancer-predisposing syndrome
GLikely pathogenic
LOC129933695, MSH2
Deletion
(genic upstream transcript variant)
Hereditary nonpolyposis colorectal neoplasms
GLikely pathogenic
LOC129933695, MSH2
Deletion
Lynch syndrome
GPathogenic
LOC129933695, MSH2
Deletion
Lynch syndrome
GPathogenic
MSH2
Single nucleotide variant
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
not provided
GLikely benign
LOC129933695, MSH2
Deletion
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Duplication
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Deletion
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
LOC129933695, MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Microsatellite
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GLikely benign
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Deletion
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
Hereditary cancer-predisposing syndrome
GUncertain significance
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