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Items: 84

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABI1, ACBD5
+1221 more
Copy number gain
See cases
GBenign
ABI1, ACBD5
+376 more
Copy number gain
See cases
GLikely pathogenic
ZNF438
(S814R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(S823C +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(S813A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZNF438
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZNF438
(E740D +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R777Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ZNF438
(R787W +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(M784V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(W771R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(P763R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(Q709P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(P736T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(G696R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(H731R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(A712T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R697K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(D700N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(H696N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(Q646L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(P635A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(K579R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(M565L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(A589V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(H536R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R562H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(G549S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(M544T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(G499R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R528Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(S526C +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(Y525S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R522G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(H511N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(N503S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R459S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(S463A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(L412F +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(G418A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R409K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ZNF438
(K339E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R338Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(R387W +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(L375P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(P363A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(V351G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(D276N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(G267D +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF438
(T226A +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF438
(N261S +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF438
(T198A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(I246L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(L226R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(L236P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(T224I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(P207S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(N147S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(P153A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(P93S +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF438
(M101L +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZNF438
(R100T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(A103T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(L82V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(K61R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(S18C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF438
(R48H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF438
(G17S +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ZNF438
(R25K +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ZNF438
(T21I +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ZNF438
(I17F +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ZNF438
(D11E)
Single nucleotide variant
(missense variant +2 more)
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
LYZL2, MAP3K8
+3 more
Duplication
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
ARHGAP12, CCDC7
+9 more
Copy number loss
not provided
GPathogenic
MTPAP, MAP3K8
+3 more
Copy number gain
not provided
GUncertain significance
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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