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Items: 1 to 100 of 382

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APBA2, ARHGAP11A
+264 more
Copy number gain
See cases
GPathogenic
APBA2, ARHGAP11B
+254 more
Copy number gain
See cases
GPathogenic
APBA2, ARHGAP11B
+228 more
Duplication
Autism
GPathogenic
APBA2, ARHGAP11B
+227 more
Copy number gain
15q11q13 microduplication syndrome
GPathogenic
APBA2, ARHGAP11B
+205 more
Copy number gain
See cases
GPathogenic
APBA2, ARHGAP11A-DT
+212 more
Copy number gain
See cases
GPathogenic
ACTC1, APBA2
+363 more
Copy number gain
See cases
GPathogenic
APBA2, ARHGAP11B
+205 more
Copy number loss
See cases
GPathogenic
ACTC1, APBA2
+346 more
Copy number loss
See cases
GPathogenic
APBA2, ARHGAP11A-DT
+212 more
Copy number gain
See cases
GPathogenic
APBA2, ARHGAP11B
+205 more
Copy number gain
See cases
GPathogenic
SNORD115-20, SNORD115-21
+314 more
Copy number loss
See cases
GPathogenic
FAN1, GOLGA8T
+61 more
Copy number loss
See cases
GPathogenic
LOC106783506, LOC110121498
+52 more
Copy number gain
See cases
GUncertain significance
APBA2, ARHGAP11B
+52 more
Copy number loss
See cases
GPathogenic
APBA2, ARHGAP11B
+52 more
Copy number gain
See cases
GUncertain significance
APBA2, ARHGAP11B
+51 more
Copy number loss
See cases
GPathogenic
APBA2, ARHGAP11A-DT
+58 more
Copy number gain
See cases
GUncertain significance
APBA2, ARHGAP11B
+51 more
Copy number gain
See cases
GUncertain significance
ARHGAP11B, ARHGAP11B-DT
+37 more
Copy number gain
See cases
GUncertain significance
FAN1, GOLGA8H
+43 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+36 more
Copy number gain
See cases
GUncertain significance
ARHGAP11A-DT, ARHGAP11B
+41 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number gain
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+34 more
Deletion
Schizophrenia
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number gain
See cases
GPathogenic
ARHGAP11A-DT, ARHGAP11B
+41 more
Copy number gain
See cases
GUncertain significance
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number loss
See cases
GPathogenic
ARHGAP11A-DT, ARHGAP11B
+41 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+38 more
Copy number gain
See cases
Gconflicting data from submitters
ARHGAP11A, ARHGAP11A-DT
+43 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+36 more
Copy number gain
See cases
GPathogenic
LOC106736468, LOC106736469
+38 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number gain
See cases
GUncertain significance
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number loss
See cases
GPathogenic
ARHGAP11A, ARHGAP11A-DT
+43 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+34 more
Copy number gain
See cases
GUncertain significance
ARHGAP11A-DT, ARHGAP11B
+41 more
Copy number gain
See cases
Gconflicting data from submitters
ARHGAP11B, ARHGAP11B-DT
+35 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+35 more
Copy number gain
See cases
GUncertain significance
ARHGAP11A-DT, ARHGAP11B
+38 more
Copy number gain
See cases
GConflicting classifications of pathogenicity
ARHGAP11B, ARHGAP11B-DT
+31 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+35 more
Copy number gain
See cases
Gconflicting data from submitters
LOC130056726, LOC130056727
+31 more
Duplication
Schizophrenia
GLikely pathogenic
LOC106736465, ARHGAP11B
+31 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+31 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+31 more
Copy number gain
See cases
GUncertain significance
ARHGAP11A, ARHGAP11A-DT
+40 more
Copy number gain
See cases
GUncertain significance
ARHGAP11B, ARHGAP11B-DT
+31 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+31 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+29 more
Deletion
Autism
GPathogenic
LOC106736480, LOC106783506
+29 more
Duplication
Schizophrenia
GLikely pathogenic
LINC02352, LOC106736468
+29 more
Deletion
Autism
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+28 more
Copy number loss
See cases
GPathogenic
ARHGAP11A-DT, ARHGAP11B
+35 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, ARHGAP11B-DT
+27 more
Copy number gain
See cases
Gconflicting data from submitters
KLF13, ARHGAP11B
+27 more
Copy number gain
See cases
GUncertain significance
LOC129390680, LOC130056726
+25 more
Deletion
Chromosome 15q13.3 microdeletion syndrome
GPathogenic
LOC129390679, LOC129390680
+24 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, CHRNA7
+24 more
Copy number gain
See cases
GUncertain significance
LINC02352, ARHGAP11B
+24 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, CHRNA7
+28 more
Copy number gain
See cases
GPathogenic
ARHGAP11B, CHRNA7
+24 more
Copy number loss
See cases
GPathogenic
LINC02352, ARHGAP11B
+24 more
Copy number gain
See cases
GUncertain significance
ARHGAP11A, ARHGAP11A-DT
+33 more
Copy number loss
See cases
GPathogenic
LINC02352, ARHGAP11B
+24 more
Copy number gain
See cases
GUncertain significance
ARHGAP11B, CHRNA7
+23 more
Copy number loss
See cases
GPathogenic
ARHGAP11B, CHRNA7
+24 more
Copy number gain
See cases
GUncertain significance
CHRNA7, FAN1
+27 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+23 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+23 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+23 more
Copy number gain
See cases
GUncertain significance
CHRNA7, FAN1
+23 more
Copy number gain
See cases
GUncertain significance
CHRNA7, FAN1
+23 more
Copy number loss
See cases
GPathogenic
ARHGAP11A-DT, CHRNA7
+30 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+23 more
Copy number gain
See cases
GUncertain significance
LOC130056727, MIR211
+23 more
Copy number loss
See cases
GPathogenic
ARHGAP11A-DT, GOLGA8O
+29 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+22 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+22 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+22 more
Copy number gain
See cases
Gconflicting data from submitters
CHRNA7, FAN1
+22 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+22 more
Copy number loss
See cases
GPathogenic
LINC03034, CHRNA7
+22 more
Copy number gain
See cases
GPathogenic
ARHGAP11A-DT, CHRNA7
+29 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+22 more
Copy number loss
See cases
GPathogenic
CHRNA7, FAN1
+21 more
Copy number gain
Anomalous pulmonary venous return
GUncertain significance
CHRNA7, LOC106736477
+3 more
Copy number gain
See cases
GUncertain significance
CHRNA7, LOC106736477
+4 more
Copy number loss
See cases
GPathogenic
CHRNA7, LOC106736477
+4 more
Copy number gain
See cases
GUncertain significance
CHRNA7, LOC125078053
+3 more
Copy number gain
See cases
GLikely benign
CHRNA7, LOC125078053
+3 more
Copy number loss
See cases
GPathogenic
CHRNA7, LOC125078053
+3 more
Copy number gain
See cases
GUncertain significance
CHRNA7, LOC125078053
+3 more
Copy number gain
See cases
GUncertain significance
CHRNA7, LOC125078053
+3 more
Duplication
15q11q13 microduplication syndrome
GUncertain significance
CHRNA7, LOC125078053
+3 more
Copy number gain
See cases
GBenign/Likely benign
CHRNA7, LOC125078053
+2 more
Copy number gain
See cases
GBenign
CHRNA7, LOC125078053
+3 more
Copy number gain
See cases
Gconflicting data from submitters
LOC130056727, CHRNA7
+3 more
Copy number gain
See cases
GBenign
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