"GeneDx"[submitter] AND "ZNRF1"[gene] - ClinVar

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59514	GRCh38/hg38 16q22.1-23.1(chr16:69918076-76723348)x1	AARS1, ADAT1 +295 more	Copy number loss	See cases	GPathogenic
Select item 59515	GRCh38/hg38 16q22.3-23.3(chr16:73049467-82576326)x1	LOC112486211, LOC112486212 +360 more	Copy number loss	See cases	GPathogenic
Select item 59996	GRCh38/hg38 16q22.3-23.1(chr16:73917167-75319927)x3	BCAR1, CFDP1 +75 more	Copy number gain	See cases	GUncertain significance
Select item 146037	GRCh38/hg38 16q23.1(chr16:74881191-75310294)x1	BCAR1, CFDP1 +42 more	Copy number loss	See cases	GUncertain significance
Select item 1282161	NC_000016.10:g.74998834G>C	LOC130059400, ZNRF1	Single nucleotide variant	not provided	GBenign
Select item 1236427	NM_032268.5(ZNRF1):c.-273C>T	ZNRF1	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1268577	NM_032268.5(ZNRF1):c.424+140A>G	ZNRF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273025	NM_032268.5(ZNRF1):c.424+221C>A	ZNRF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250248	NM_032268.5(ZNRF1):c.425-209C>T	ZNRF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230874	NM_032268.5(ZNRF1):c.626+140A>G	ZNRF1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253554	GRCh37/hg19 16q23.1-24.3(chr16:74872514-90274440)x3	ACSF3, ADAD2 +127 more	Copy number gain	See cases	GPathogenic