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Items: 1 to 100 of 5044

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABHD1, ACP1
+1047 more
Copy number gain
See cases
GPathogenic
ABCG5, ABCG8
+1631 more
Copy number gain
See cases
GPathogenic
ABCG5, ABCG8
+1400 more
Copy number gain
See cases
GPathogenic
LOC126806252, LOC126806253
+2457 more
Copy number gain
See cases
GBenign
ALK, CLIP4
+37 more
Copy number gain
See cases
GUncertain significance
ALK, CLIP4
+37 more
Copy number gain
See cases
GUncertain significance
ALK, CLIP4
+35 more
Copy number gain
See cases
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma Susceptibility
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GBenign
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GBenign
ALK
Duplication
(3 prime UTR variant)
Neuroblastoma Susceptibility
GUncertain significance
ALK
Duplication
(3 prime UTR variant)
not provided
+1 more
GBenign
ALK
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GBenign/Likely benign
ALK
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GBenign
ALK
Single nucleotide variant
(3 prime UTR variant)
Neuroblastoma, susceptibility to, 3
GBenign
ALK
Deletion
(frameshift variant)
not provided
+1 more
GUncertain significance
ALK, LOC105374389
+2 more
Duplication
Neuroblastoma, susceptibility to, 3
GUncertain significance
LOC122756683, ALK
Duplication
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Deletion
(frameshift variant +1 more)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+1 more
GLikely benign
ALK
Single nucleotide variant
(stop lost)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(P552L +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(P1620S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
ALK
(G551V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(G1619R +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
Duplication
(inframe_insertion)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(P1618S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(Q1617H +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(Q1617R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
(Q549* +1 more)
Single nucleotide variant
(nonsense)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(M1615I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(M1615R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
(M1615T +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
ALK
(S546T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
(S1614C +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(N545K +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(K1612N +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(S1611fs +1 more)
Deletion
(frameshift variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(K1612N +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
ALK
(K1612Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
(S1611N +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(S1611I +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(K1610N +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(L1609P +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(L1609M +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(L541V +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+1 more
GLikely benign
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(E1605K +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
(Y536* +1 more)
Single nucleotide variant
(nonsense)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+2 more
GLikely benign
ALK
(Y1604* +1 more)
Single nucleotide variant
(nonsense)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(Y1604C +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
ALK
(Y1604H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+1 more
GConflicting classifications of pathogenicity
ALK
(H1603L +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(H535Y +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(G1602A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(G1602S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(A1601T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(G532R +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
ALK
(P1599H +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ALK
(P1599S +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ALK
(A1598V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
+1 more
GLikely benign
ALK
(L525fs +1 more)
Deletion
(frameshift variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(T529A +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(A528S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
(A1596T +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
ALK
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
ALK
(A1595D +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(A1595V +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(A527S +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
(E1594K +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+1 more
GLikely benign
ALK
(L525S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
GLikely benign
ALK
(P1592L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
ALK
(P524T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
ALK
(L523F +1 more)
Single nucleotide variant
(missense variant)
Neuroblastoma, susceptibility to, 3
GUncertain significance
ALK
Single nucleotide variant
(synonymous variant)
Neuroblastoma, susceptibility to, 3
+1 more
GLikely benign
ALK
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
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