"GeneDx"[submitter] AND "RPL21"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59853	GRCh38/hg38 13q11-13.3(chr13:18676442-37656039)x3	LOC130009419, LOC130009420 +567 more	Copy number gain	See cases	GPathogenic
Select item 59861	GRCh38/hg38 13q12.11-12.3(chr13:18958091-31090460)x3	LOC130009490, LOC130009491 +416 more	Copy number gain	See cases	GPathogenic
Select item 145957	GRCh38/hg38 13q12.13-12.3(chr13:26965244-30097858)x3	CDX2, FLT1 +123 more	Copy number gain	See cases	GLikely pathogenic
Select item 1243002	NM_000982.4(RPL21):c.-12-91C>T	RPL21	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270905	NM_000982.4(RPL21):c.67+9G>A	RPL21	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237877	NM_000982.4(RPL21):c.67+61A>G	RPL21	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287865	NM_000982.4(RPL21):c.130-310dup	RPL21	Duplication (intron variant)	not provided	GBenign
Select item 1235163	NM_000982.4(RPL21):c.130-69G>A	RPL21	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271809	NM_000982.4(RPL21):c.159C>T (p.Pro53=)	RPL21	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1233915	NM_000982.4(RPL21):c.243-222A>G	RPL21	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227239	NC_000013.11:g.27256682del	RPL21	Deletion	not provided	GBenign
Select item 1225745	NC_000013.11:g.27256811A>C	RPL21	Single nucleotide variant	not provided	GBenign
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic