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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTR1B, ADRA2B
+550 more
Copy number gain
See cases
GPathogenic
ACOXL, BUB1
+241 more
Copy number gain
See cases
GPathogenic
ACOXL, ACOXL-AS1
+154 more
Copy number gain
See cases
GUncertain significance
CCDC138, CD8B2
+99 more
Copy number gain
See cases
GUncertain significance
CCDC138, EDAR
+61 more
Copy number gain
See cases
GUncertain significance
LIMS3, LIMS3-LOC440895
+33 more
Copy number gain
Autism spectrum disorder
GUncertain significance
LIMS3-LOC440895, LIMS4
+13 more
Copy number loss
See cases
GBenign
LIMS4, LINC01106
+13 more
Copy number gain
See cases
GLikely benign
LIMS4, LINC01106
+12 more
Copy number loss
See cases
GBenign
LIMS4, LINC01106
+12 more
Copy number gain
See cases
GLikely benign
LIMS4, LINC01106
+12 more
Copy number loss
See cases
GBenign
LIMS4, LINC01106
+11 more
Copy number gain
See cases
GBenign
LIMS4, LINC01106
+11 more
Copy number loss
See cases
GBenign
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