C0040822[trait identifier] AND "Department of Molecular and Human Gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 180225	NC_000006.11:g.(117961791_117961792)_(118280043_118280044)del	LOC101927919, LOC126859772 +5 more	Deletion	Intellectual disability +2 more	GPathogenic
Select item 180226	NC_000006.11:g.(117971549_117971550)_(118218719_118218720)del	LOC101927919, LOC129389624 +3 more	Deletion	Intellectual disability +2 more	GPathogenic
Select item 180227	NC_000006.11:g.(116681080_116735056)_(119687719_119775014)del	ASF1A, CALHM4 +22 more	Deletion	Tremor +3 more	GPathogenic

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