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Items: 1 to 100 of 285

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL17RA, LINC01640
+2088 more
Copy number gain
See cases
GPathogenic
LOC130067034, LOC130067035
+535 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
AIFM3, ARVCF
+378 more
Copy number loss
See cases
GPathogenic
AIFM3, BCR
+265 more
Copy number loss
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+823 more
Copy number gain
See cases
GPathogenic
BCR, C22orf15
+229 more
Copy number gain
See cases
GUncertain significance
BCR, CCDC116
+177 more
Copy number gain
See cases
GPathogenic
BCR, CCDC116
+180 more
Copy number loss
See cases
GPathogenic
BCR, C22orf15
+223 more
Copy number loss
See cases
GPathogenic
LOC129929044, LOC129929045
+176 more
Copy number loss
See cases
GPathogenic
BCR, C22orf15
+223 more
Copy number loss
See cases
GPathogenic
BCR, CCDC116
+179 more
Copy number loss
See cases
GPathogenic
BCR, CCDC116
+179 more
Copy number gain
See cases
GPathogenic
BCR, C22orf15
+222 more
Copy number loss
See cases
GPathogenic
BCR, C22orf15
+227 more
Copy number loss
See cases
GPathogenic
BCR, CCDC116
+168 more
Copy number loss
See cases
GPathogenic
DDTL, DERL3
+164 more
Duplication
Schizophrenia
GLikely pathogenic
IGLL5, IGLV2-11
+85 more
Deletion
Schizophrenia
GLikely pathogenic
BCR, GNAZ
+81 more
Copy number loss
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+163 more
Copy number gain
See cases
GUncertain significance
BCR, GNAZ
+81 more
Copy number loss
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
LOC129929045, LOC130067057
+81 more
Copy number loss
See cases
GUncertain significance
BCR, GNAZ
+81 more
Copy number loss
See cases
GPathogenic
BCR, GNAZ
+82 more
Copy number gain
See cases
GUncertain significance
BCR, GNAZ
+81 more
Copy number loss
See cases
GLikely benign
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
+160 more
Copy number gain
See cases
GUncertain significance
BCR, GNAZ
+80 more
Copy number loss
See cases
GUncertain significance
BCR, GNAZ
+80 more
Copy number gain
See cases
GUncertain significance
BCR, GNAZ
+80 more
Copy number gain
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+160 more
Copy number gain
See cases
GConflicting classifications of pathogenicity
LOC130067089, LOC130067090
+81 more
Copy number loss
See cases
GPathogenic
DRICH1, FAM230I
+162 more
Copy number gain
See cases
GUncertain significance
IGLV3-22, IGLV3-25
+160 more
Copy number gain
See cases
GUncertain significance
BCR, GNAZ
+82 more
Copy number loss
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+157 more
Copy number gain
See cases
GUncertain significance
BCR, GNAZ
+73 more
Copy number loss
See cases
GPathogenic
ADORA2A, ADORA2A-AS1
+124 more
Copy number gain
See cases
GUncertain significance
BCR
(E36D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(E46D)
Single nucleotide variant
(missense variant)
not provided
GBenign
BCR
Single nucleotide variant
(synonymous variant)
not provided
GBenign
BCR
(Y70C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(R72W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(R78W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A80V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A87G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A94V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(G104R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A115V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(R132L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(R132P)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
BCR
(A152T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A152V)
Single nucleotide variant
(missense variant)
not provided
GBenign
BCR
(G166D)
Single nucleotide variant
(missense variant)
not provided
GBenign
BCR
(Q167P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(H184Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(D193N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(K194R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
Acute lymphoid leukemia
+2 more
GBenign/Likely benign
BCR
(M210L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A219T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(P229S)
Single nucleotide variant
(missense variant)
Acute lymphoid leukemia
+1 more
GUncertain significance
BCR
(Y231N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(R232W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(P253S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(P253L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(R254C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(A263T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(P273H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GBenign
BCR
Single nucleotide variant
(synonymous variant)
not provided
GBenign
BCR
(Q277H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(K293E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(K293R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(P295Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(K307R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(R308C)
Single nucleotide variant
(missense variant)
not provided
GBenign
BCR
(S317Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(D323N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(F345del)
Deletion
(inframe_deletion)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BCR
(M362T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(S381N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
Single nucleotide variant
(synonymous variant)
Acute lymphoid leukemia
+1 more
GUncertain significance
BCR
(P396L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BCR
(I413M)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
BCR
(D425E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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