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Links from Gene

Items: 1 to 100 of 188

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AIFM3, ARVCF
+174 more
Copy number gain
Microcephaly-digital anomalies-intellectual disability syndrome
GPathogenic
AIFM3, ARVCF
+169 more
Copy number loss
DiGeorge syndrome
GPathogenic
LOC130066999, LOC130067004
+170 more
Deletion
Velocardiofacial syndrome
GPathogenic
LOC130066967, TSSK2
+170 more
Duplication
Chromosome 22q11.2 microduplication syndrome
GPathogenic
AIFM3, ARVCF
+190 more
Deletion
22q11.2 deletion syndrome
GPathogenic
LOC125424386, LOC125424387
+169 more
Duplication
Chromosome 22q11.2 microduplication syndrome
GPathogenic
LINC00896, LINC01311
+169 more
Deletion
Chromosome 22q11.2 deletion syndrome, distal
GPathogenic
LOC130066986, LOC130066994
+170 more
Deletion
Velocardiofacial syndrome
GPathogenic
DGCR5, DGCR6
+3 more
Deletion
Proline dehydrogenase deficiency
GPathogenic
FAM246C, FAM247A
+179 more
Duplication
Autism
GPathogenic
DGCR2, DGCR5
+107 more
Duplication
Autism
GPathogenic
LOC132090919, LOC132090920
+175 more
Deletion
Schizophrenia
GPathogenic
MIR185, MIR3618
+109 more
Deletion
Schizophrenia
GPathogenic
LOC130067012, LOC130067013
+180 more
Deletion
Schizophrenia
GPathogenic
AIFM3, ARVCF
+175 more
Deletion
Schizophrenia
GPathogenic
AIFM3, ARVCF
+181 more
Deletion
Schizophrenia
GPathogenic
PI4KA, PRODH
+192 more
Deletion
Schizophrenia
GPathogenic
AIFM3, ARVCF
+196 more
Deletion
Schizophrenia
GPathogenic
AIFM3, ARVCF
+195 more
Deletion
Schizophrenia
GPathogenic
ARVCF, C22orf39
+119 more
Copy number loss
See cases
GPathogenic
ARVCF, C22orf39
+120 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+195 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+186 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+190 more
Copy number loss
See cases
GPathogenic
ARVCF, C22orf39
+119 more
Copy number gain
See cases
GPathogenic
CLDN5, AIFM3
+189 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number gain
See cases
GPathogenic
ARVCF, C22orf39
+106 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+189 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+195 more
Copy number gain
See cases
GPathogenic
LOC130067005, LOC130067006
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+186 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+189 more
Copy number gain
See cases
GPathogenic
DGCR5, DGCR6
+4 more
Deletion
Normal pregnancy
Gnot provided
ARVCF, C22orf39
+106 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
LOC130066971, LOC130066972
+185 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
LOC130067008, LOC130067009
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+184 more
Copy number loss
See cases
GUncertain significance
DGCR5, DGCR6
+15 more
Copy number gain
See cases
GLikely benign
LOC132090631, LOC132090632
+196 more
Copy number loss
See cases
GPathogenic
LOC130066953, LOC130066954
+191 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+184 more
Copy number loss
See cases
GUncertain significance
LINC01311, LINC01637
+195 more
Copy number gain
See cases
GPathogenic
ARVCF, C22orf39
+119 more
Copy number loss
See cases
GPathogenic
ADA2, ATP6V1E1
+121 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+187 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+187 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
ARVCF, C22orf39
+106 more
Copy number loss
See cases
GPathogenic
ARVCF, C22orf39
+147 more
Copy number loss
See cases
GPathogenic
LOC130066989, LOC130066990
+106 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+170 more
Copy number loss
See cases
GUncertain significance
LOC112694767, LOC114004361
+187 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+195 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+186 more
Copy number gain
See cases
GPathogenic
CLTCL1, DGCR11
+19 more
Copy number gain
See cases
GUncertain significance
AIFM3, ARVCF
+378 more
Copy number loss
See cases
GPathogenic
ARVCF, C22orf39
+106 more
Copy number gain
See cases
GPathogenic
LOC130067004, LOC130067005
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
DGCR5, HSERVPRODH
+2 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number gain
See cases
GPathogenic
DGCR5, DGCR6
+5 more
Copy number gain
See cases
GLikely benign
DGCR5, DGCR6
+3 more
Copy number gain
See cases
GLikely benign
LOC130066994, LOC130066995
+287 more
Copy number gain
See cases
GPathogenic
LOC130067010, LOC130067011
+185 more
Copy number gain
See cases
GPathogenic
DGCR5, DGCR6
+15 more
Copy number gain
See cases
GLikely benign
AIFM3, ARVCF
+186 more
Copy number loss
See cases
GPathogenic
DGCR5, DGCR6
+15 more
Copy number loss
See cases
GLikely benign
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
LINC00895, LINC00896
+195 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
COMT, CLTCL1
+107 more
Copy number gain
See cases
GPathogenic
LINC01637, LINC02891
+189 more
Copy number loss
See cases
GPathogenic
LOC130067014, LOC130067015
+185 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+194 more
Copy number gain
See cases
GUncertain significance
GSC2, HIRA
+31 more
Copy number gain
See cases
GUncertain significance
AIFM3, ARVCF
+186 more
Copy number loss
See cases
GPathogenic
CLTCL1, DGCR11
+38 more
Copy number gain
See cases
GPathogenic
ARVCF, C22orf39
+107 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+181 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+195 more
Copy number loss
See cases
GPathogenic
AIFM3, ARVCF
+185 more
Copy number loss
See cases
GPathogenic
ARVCF, C22orf39
+109 more
Copy number loss
See cases
GPathogenic
LINC01637, LOC114004361
+185 more
Copy number loss
See cases
GUncertain significance
LOC130067003, LOC130067004
+192 more
Copy number gain
See cases
GPathogenic
AIFM3, ARVCF
+179 more
Copy number gain
See cases
GPathogenic
ARVCF, C22orf39
+106 more
Copy number gain
See cases
GPathogenic
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