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Items: 76

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACBD7, ACBD7-DCLRE1CP1
+837 more
Copy number gain
See cases
GPathogenic
ABI1, ACBD5
+1221 more
Copy number gain
See cases
GBenign
ABI1, ACBD5
+376 more
Copy number gain
See cases
GLikely pathogenic
ARMC3
(K7T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(E10V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(T29S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(M33I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(E70G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(T88I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
Single nucleotide variant
(synonymous variant +1 more)
EBV-positive nodal T- and NK-cell lymphoma
GLikely benign
ARMC3
(V124L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(L152I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(P164L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(S170F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(A192S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(A211V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(I238V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(C260S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ARMC3
(Q292R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(K38R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
Single nucleotide variant
(splice donor variant)
Stuttering, familial persistent, 4
GUncertain significance
ARMC3
(V322L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(S327F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(A335T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(D88V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(Q356L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(Q97E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(N369S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(R110W +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARMC3
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
ARMC3
(A131S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(P139T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(R148Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(V158I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(A163V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(P167L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(I440L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(M441I +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ARMC3
(I182V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(L185M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(V207A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(T211N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(E511K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(V268I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(N545T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(T296S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(Y561C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(I304T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(G308V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(Y573H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(I578T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(G581S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(E326K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(R599Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(T676I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(W418L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(P455L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(M725T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(E507Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(F778S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(I548T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(G549C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(G814S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(G814V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(M828I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(D569H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC3
(R834W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGAP5, CRTAC1
+682 more
Copy number gain
Distal trisomy 10q
GPathogenic
ABRAXAS2, CHCHD1
+673 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
ARMC3, BMI1
+6 more
Copy number gain
not provided
GUncertain significance
ABI1, ACBD5
+111 more
Copy number gain
not specified
GPathogenic
ARL5B, LARP4B
+180 more
Copy number gain
Mosaic supernumerary isodicentric chromosome 10
Gnot provided
ABI1, ACBD5
+205 more
Copy number gain
See cases
GPathogenic
INA, INPP5A
+721 more
Copy number gain
See cases
GPathogenic
A1CF, ABCC2
+721 more
Copy number gain
See cases
GPathogenic
A1CF, ABCC2
+722 more
Copy number gain
See cases
GPathogenic
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