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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	LOC123453201, LOC123453202 +1450 more	Copy number gain	See cases	GPathogenic
Select item 57984	GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3	LOC132088897, LOC132088898 +1201 more	Copy number gain	See cases	GPathogenic
Select item 57868	GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1	MIR944, MUC20 +557 more	Copy number loss	See cases	GPathogenic
Select item 58000	GRCh38/hg38 3q29(chr3:194424496-198168758)x3	RUBCN, SENP5 +264 more	Copy number gain	See cases	GPathogenic
Select item 1687678	NM_198565.3(NRROS):c.863G>A (p.Arg288Gln)	NRROS (R288Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1328539	NM_198565.3(NRROS):c.1222A>C (p.Asn408His)	NRROS (N408H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 253577	GRCh37/hg19 3q29(chr3:195690241-197299811)x1	NRROS, SENP5 +19 more	Copy number loss	See cases	GPathogenic
Select item 253357	GRCh37/hg19 3q29(chr3:196281672-197681798)x3	PAK2, PIGZ +15 more	Copy number gain	See cases	GLikely pathogenic

ClinVar