"GeneDx"[submitter] AND "NME4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58594	GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3	LOC112340388, LOC112441449 +821 more	Copy number gain	See cases	GPathogenic
Select item 58595	GRCh38/hg38 16p13.3(chr16:29941-2560460)x3	ABCA3, AMDHD2 +356 more	Copy number gain	See cases	GPathogenic
Select item 58597	GRCh38/hg38 16p13.3(chr16:46766-3214623)x3	ARHGDIG, ATP6V0C +482 more	Copy number gain	See cases	GPathogenic
Select item 145053	GRCh38/hg38 16p13.3(chr16:350651-396961)x3	AXIN1, LOC100134368 +11 more	Copy number gain	See cases	GBenign
Select item 145052	GRCh38/hg38 16p13.3(chr16:350651-396961)x4	AXIN1, LOC100134368 +11 more	Copy number gain	See cases	GBenign
Select item 1266035	NM_005009.3(NME4):c.328-73G>C	NME4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253809	GRCh37/hg19 16p13.3(chr16:239130-841725)x3	STUB1, CIAO3 +32 more	Copy number gain	See cases	GUncertain significance
Select item 253755	GRCh37/hg19 16p13.3(chr16:450686-1007236)x3	MSLN, PRR35 +27 more	Copy number gain	See cases	GUncertain significance
Select item 253622	GRCh37/hg19 16p13.3(chr16:72769-1511716)x1	CCDC154, CCDC78 +61 more	Copy number loss	See cases	GPathogenic

ClinVar