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Items: 1 to 100 of 274

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129931348, LOC129931349
+212 more
Copy number gain
See cases
GPathogenic
CD160, ACP6
+177 more
Copy number loss
See cases
GPathogenic
LOC129931342, LOC129931343
+182 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+178 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+177 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+178 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+168 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number loss
See cases
GLikely pathogenic
ACP6, ANKRD34A
+153 more
Copy number loss
See cases
GPathogenic
LOC126805853, LOC126805854
+153 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+153 more
Copy number gain
See cases
GPathogenic
ANKRD34A, ANKRD35
+73 more
Copy number loss
See cases
GBenign
ACP6, ANKRD34A
+143 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number loss
See cases
GPathogenic
LOC101927468, LOC106783502
+143 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic
LOC129931329, LOC129931330
+143 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+129 more
Copy number gain
See cases
GPathogenic
ACP6, ANKRD34A
+136 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic
MIR5087, MIR6077
+143 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+143 more
Copy number gain
See cases
GPathogenic/Likely pathogenic
ACP6, ANKRD34A
+133 more
Copy number gain
See cases
GPathogenic
LOC101927468, LOC106783502
+133 more
Copy number gain
See cases
GPathogenic
ANKRD34A, ANKRD35
+61 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+67 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+61 more
Copy number gain
See cases
GUncertain significance
ANKRD34A, ANKRD35
+61 more
Copy number gain
See cases
GUncertain significance
ACP6, ANKRD34A
+129 more
Copy number gain
See cases
GPathogenic
RNVU1-6, RNVU1-7
+118 more
Deletion
Schizophrenia
GPathogenic
LOC129931347, LOC129931348
+104 more
Deletion
Schizophrenia
GPathogenic
ANKRD34A, ANKRD35
+66 more
Copy number gain
See cases
GConflicting classifications of pathogenicity
ACP6, ANKRD34A
+115 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+130 more
Deletion
Schizophrenia
GPathogenic
ACP6, ANKRD34A
+127 more
Duplication
Schizophrenia
GLikely pathogenic
LOC129931348, LOC129931349
+52 more
Duplication
Schizophrenia
GLikely pathogenic
ANKRD34A, ANKRD35
+52 more
Deletion
Schizophrenia
GLikely pathogenic
ANKRD34A, ANKRD35
+52 more
Duplication
Schizophrenia
GLikely pathogenic
GPR89B, LOC129931326
+123 more
Deletion
Radial aplasia-thrombocytopenia syndrome
GLikely pathogenic
ANKRD34A, ANKRD35
+43 more
Copy number gain
See cases
GUncertain significance
ANKRD34A, ANKRD35
+55 more
Copy number loss
See cases
GLikely pathogenic
ANKRD34A, ANKRD35
+54 more
Copy number loss
See cases
GLikely benign
ACP6, ANKRD34A
+123 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+52 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+44 more
Copy number loss
See cases
GPathogenic
ACP6, ANKRD34A
+123 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+52 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+61 more
Copy number gain
See cases
GPathogenic
ANKRD34A, ANKRD35
+61 more
Copy number gain
See cases
GPathogenic
ANKRD34A, ANKRD35
+61 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+43 more
Copy number gain
See cases
GUncertain significance
ANKRD34A, ANKRD35
+54 more
Copy number loss
See cases
GUncertain significance
ANKRD34A, ANKRD35
+50 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+42 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+42 more
Copy number loss
See cases
GUncertain significance
ANKRD34A, ANKRD35
+42 more
Copy number gain
See cases
Gconflicting data from submitters
ANKRD34A, ANKRD35
+41 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+50 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+35 more
Copy number gain
See cases
GUncertain significance
ANKRD34A, ANKRD35
+41 more
Copy number gain
See cases
GBenign
ANKRD34A, ANKRD35
+41 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+50 more
Copy number loss
See cases
GUncertain significance
TXNIP, ANKRD34A
+42 more
Copy number loss
See cases
GLikely pathogenic
ANKRD34A, ANKRD35
+49 more
Copy number loss
See cases
GPathogenic
ANKRD34A, ANKRD35
+53 more
Copy number gain
See cases
GPathogenic
ANKRD34A, ANKRD35
+52 more
Copy number gain
See cases
GLikely pathogenic
ANKRD34A, ANKRD35
+40 more
Copy number loss
See cases
GUncertain significance
ANKRD34A, ANKRD35
+47 more
Copy number loss
Radial aplasia-thrombocytopenia syndrome
GPathogenic
ANKRD35
(N990D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(H896Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(R981Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ANKRD35
(Y882C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(L864P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(R858Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(R948W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(A856P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(E932Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(A832V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(Y770C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(G718R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(Q715H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(Q784E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(N664K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(R739P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(Q629R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ANKRD35
(L603R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ANKRD35
(M592V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ANKRD35
(R580Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ANKRD35
(P568A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(R564G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(R548P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(E614Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD35
(A508S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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