"GeneDx"[submitter] AND "GDPD3"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58626	GRCh38/hg38 16p12.2-11.2(chr16:23047969-30632245)x3	DCTPP1, DOC2A +409 more	Copy number gain	See cases	GPathogenic
Select item 152605	GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3	LOC130058732, LOC130058733 +504 more	Copy number gain	See cases	GPathogenic
Select item 151637	GRCh38/hg38 16p12.1-11.2(chr16:27311746-31193406)x3	ZNF747, ZNF747-DT +378 more	Copy number gain	See cases	GPathogenic
Select item 58735	GRCh38/hg38 16p12.1-11.2(chr16:28456967-30295107)x1	ALDOA, APOBR +186 more	Copy number loss	See cases	GPathogenic
Select item 60372	GRCh38/hg38 16p11.2(chr16:28531783-30183432)x1	LOC130058756, LOC130058757 +170 more	Copy number loss	See cases	GPathogenic
Select item 146013	GRCh38/hg38 16p11.2(chr16:29909613-31438697)x3	LOC130058889, LOC130058890 +207 more	Copy number gain	See cases	GPathogenic
Select item 512692	NM_024307.3(GDPD3):c.819+9G>T	GDPD3	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 253669	GRCh37/hg19 16p11.2(chr16:29646320-30197341)x3	MAZ, TLCD3B +25 more	Copy number gain	See cases	GPathogenic
Select item 253535	GRCh37/hg19 16p11.2(chr16:29656684-30197341)x1	SPN, HIRIP3 +25 more	Copy number loss	See cases	GPathogenic
Select item 253525	GRCh37/hg19 16p11.2(chr16:29060171-30197341)x3	SPN, CORO1A +28 more	Copy number gain	See cases	GPathogenic
Select item 253490	GRCh37/hg19 16p11.2(chr16:29060171-30195607)x3	QPRT, ALDOA +28 more	Copy number gain	See cases	GPathogenic
Select item 253381	GRCh37/hg19 16p11.2(chr16:29656684-30197341)x3	CORO1A, ASPHD1 +25 more	Copy number gain	See cases	GPathogenic
Select item 253374	GRCh37/hg19 16p11.2(chr16:29646320-30197341)x1	GDPD3, TBX6 +25 more	Copy number loss	See cases	GPathogenic