"GeneDx"[submitter] AND "DCDC1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58858	GRCh38/hg38 11p14.3-12(chr11:22550115-38199159)x1	PAX6_HS3, PAX6_HS8 +334 more	Copy number loss	See cases	GPathogenic
Select item 145969	GRCh38/hg38 11p14.2-13(chr11:26368962-35252976)x1	LOC129390275, LOC129390276 +255 more	Copy number loss	See cases	GPathogenic
Select item 151268	GRCh38/hg38 11p13(chr11:31189295-31701133)x1	DCDC1, DNAJC24 +11 more	Copy number loss	See cases	GPathogenic
Select item 1286561	NM_001387274.1(DCDC1):c.600G>A (p.Glu200=)	DCDC1, LOC126861175	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 254003	GRCh37/hg19 11p13(chr11:31312348-31345582)x1	DCDC1	Copy number loss	See cases	GUncertain significance
Select item 253873	GRCh37/hg19 11p13(chr11:31312348-31454239)x1	DCDC1, DNAJC24 +1 more	Copy number loss	See cases	GUncertain significance
Select item 253711	GRCh37/hg19 11p13(chr11:31311902-31349768)x1	DCDC1	Copy number loss	See cases	GUncertain significance
Select item 253513	GRCh37/hg19 11p14.1-12(chr11:30615127-40606139)x1	ABTB2, APIP +41 more	Copy number loss	See cases	GPathogenic
Select item 253466	GRCh37/hg19 11p13(chr11:31284306-32458309)x1	DCDC1, DNAJC24 +6 more	Copy number loss	See cases	GPathogenic

ClinVar