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Items: 31

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862145, LOC126862146
+140 more
Copy number loss
See cases
GPathogenic
ADAM10, ALDH1A2
+163 more
Copy number loss
See cases
GPathogenic
LOC130057927, LOC130057928
+1764 more
Copy number gain
See cases
GPathogenic
ANXA2
(M292I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(M296I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(R220W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(I214V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(M189T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(K169N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(Y147F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(L121M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(V116L +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
ANXA2
(Q67H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(Y30H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANXA2
(V4I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ICE2, ANXA2
+1 more
Copy number loss
not provided
GLikely pathogenic
ADAM10, ALDH1A2
+35 more
Copy number loss
not provided
GPathogenic
ANXA2, ICE2
+1 more
Copy number loss
not provided
GUncertain significance
ADAM10, ALDH1A2
+81 more
Copy number gain
not provided
GPathogenic
CGNL1, MAPDA
+472 more
Duplication
Familial colorectal cancer
+1 more
GUncertain significance
ICE2, RORA
+1 more
Copy number gain
not provided
GUncertain significance
ANXA2, ICE2
Copy number loss
not provided
GUncertain significance
ADAM10, ALDH1A2
+76 more
Copy number gain
not provided
GPathogenic
PDIA3, PEAK1
+521 more
Duplication
not provided
GPathogenic
AAGAB, ABHD17C
+559 more
Copy number gain
See cases
GPathogenic
NOX5, NPAP1
+559 more
Copy number gain
See cases
GPathogenic
ADAM10, ALDH1A2
+17 more
Copy number loss
See cases
GPathogenic
ADAM10, ALDH1A2
+37 more
Copy number loss
See cases
GPathogenic
CHRFAM7A, CHRM5
+566 more
Copy number gain
See cases
GPathogenic
ALDH1A2, ALDH1A3
+444 more
Copy number gain
See cases
GPathogenic
WHAMM, CCNB2
+308 more
Copy number gain
not provided
GLikely pathogenic
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