"GeneDx"[submitter] AND "LOC130005200"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151263	GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3	DENND5A, DNHD1 +723 more	Copy number gain	See cases	GPathogenic
Select item 1277514	NC_000011.10:g.6603668G>A	ILK, LOC130005200	Single nucleotide variant	not provided	GBenign
Select item 671499	NM_004517.4(ILK):c.-129G>T	ILK, LOC130005200	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 383971	NM_004517.4(ILK):c.-113G>T	ILK, LOC130005200	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 385262	NM_004517.4(ILK):c.-109C>T	ILK, LOC130005200	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 137589	NM_004517.4(ILK):c.-108T>C	ILK, LOC130005200	Single nucleotide variant (5 prime UTR variant)	not specified	GBenign
Select item 381219	NM_004517.4(ILK):c.-105A>G	LOC130005200, ILK	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign

ClinVar