"Institute of Human Genetics, University of Leipzig Medical Center"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 984698	NM_001040616.3(LINS1):c.786_842del (p.Arg263_Ser281del)	LINS1	Deletion (inframe_deletion +1 more)	Intellectual disability, autosomal recessive 27	GUncertain significance
Select item 2580298	GRCh37/hg19 15q24.1-26.3(chr15:75165490-102520892)x3	ABHD17C, ABHD2 +174 more	Copy number gain	See cases	GPathogenic