"GeneDx"[submitter] AND "LOC130056358"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58526	GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3	LOC130056392, LOC130056393 +1073 more	Copy number gain	See cases	GPathogenic
Select item 57811	GRCh38/hg38 14q32.11-32.13(chr14:90255156-95274696)x1	ASB2, ATXN3 +201 more	Copy number loss	See cases	GPathogenic
Select item 58527	GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3	IGHD5-18, IGHD5-24 +881 more	Copy number gain	See cases	GPathogenic
Select item 315115	NM_177438.3(DICER1):c.-73C>T	DICER1, LOC130056358	Single nucleotide variant (5 prime UTR variant +1 more)	DICER1-related tumor predisposition +1 more	GBenign
Select item 315118	NM_177438.3(DICER1):c.-164C>T	DICER1, LOC130056358	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1223292	NM_177438.3(DICER1):c.-270G>A	DICER1, LOC130056358	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1249586	NM_177438.3(DICER1):c.-272C>T	DICER1, LOC130056358	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1198725	NM_177438.3(DICER1):c.-281G>T	DICER1, LOC130056358	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign

ClinVar