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Items: 1 to 100 of 199

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL17RA, LINC01640
+2088 more
Copy number gain
See cases
GPathogenic
LOC130067403, LOC130067404
+2088 more
Copy number gain
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+798 more
Copy number gain
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+823 more
Copy number gain
See cases
GPathogenic
DDTL, DERL3
+164 more
Duplication
Schizophrenia
GLikely pathogenic
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
DRICH1, FAM230I
+162 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+157 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+124 more
Copy number gain
See cases
GUncertain significance
LOC130067187, LOC130067188
+556 more
Copy number gain
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+84 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+81 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+81 more
Copy number gain
See cases
GLikely benign
ADORA2A, ADORA2A-AS1
+80 more
Copy number gain
See cases
GUncertain significance
LOC130067094, LOC130067095
+80 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+80 more
Copy number gain
See cases
GUncertain significance
DDT, C22orf15
+78 more
Duplication
Schizophrenia
GLikely pathogenic
LRRC75B, MIF
+78 more
Duplication
Schizophrenia
GLikely pathogenic
ADORA2A, ADORA2A-AS1
+76 more
Copy number gain
See cases
GUncertain significance
LOC130067120, LOC130067121
+76 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+76 more
Copy number gain
See cases
GUncertain significance
ADORA2A, ADORA2A-AS1
+57 more
Copy number gain
See cases
GUncertain significance
GGT1, LRRC75B
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
GGT1, LRRC75B
(A288T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(L282I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(E278Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(P274L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(Q269H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(G262S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(A231S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(R219Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(R209H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(G191R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(H178R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(V168M)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
GGT1, LRRC75B
(S144T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(R134C)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
GGT1, LRRC75B
(H124Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(T122I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(T122A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(S109P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(R95Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(P81Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(L79V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(F78I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(E48Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(E48K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(E37K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LRRC75B, GGT1
(R36C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(V32L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(E29K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1, LRRC75B
(A13T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
(L5F)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GGT1
(A29V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(V43M)
Single nucleotide variant
(missense variant)
gamma-Glutamyltransferase deficiency
GUncertain significance
GGT1
(A45T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(K52E)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Deletion
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GGT1
(G62A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(A64V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
(V109L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
GGT1
(A177V)
Single nucleotide variant
(missense variant)
not provided
GBenign
GGT1
(R182Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
GGT1
(R182P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
(T219M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GGT1
(I241V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(A243V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(R257H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(I261T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GGT1
(V272A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
GGT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
Single nucleotide variant
(intron variant)
not provided
GBenign
GGT1
(R300W)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
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