"GeneDx"[submitter] AND "LOC129935432"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	LOC129935726, LOC129935727 +1665 more	Copy number gain	See cases	GPathogenic
Select item 152538	GRCh38/hg38 2q33.1-34(chr2:199946494-209985195)x1	ABI2, ADAM23 +293 more	Copy number loss	See cases	GPathogenic
Select item 1276634	NC_000002.12:g.202376036_202376045dup	BMPR2, LOC129935432	Duplication	not provided	GBenign
Select item 1707255	NM_001204.7(BMPR2):c.-963GGC[14]	BMPR2, LOC129935432	Microsatellite (5 prime UTR variant)	not provided	GLikely benign
Select item 1238911	NM_001204.7(BMPR2):c.-963GGC[15]	BMPR2, LOC129935432	Microsatellite (5 prime UTR variant)	not provided	GBenign
Select item 333617	NM_001204.7(BMPR2):c.-963GGC[13]	BMPR2, LOC129935432	Microsatellite (5 prime UTR variant)	Pulmonary hypertension, primary, 1 +1 more	GBenign/Likely benign

ClinVar