ClinVar for Gene (Select 168448) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2657496	NM_152627.3(CDC14C):c.16C>T (p.Leu6=)	CDC14C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 148312	GRCh38/hg38 7p12.3(chr7:48734588-48997715)x1	CDC14C, LOC129389793	Copy number loss	See cases	GUncertain significance
Select item 147754	GRCh38/hg38 7p14.1-12.1(chr7:40020598-50543500)x1	ABCA13, ADCY1 +317 more	Copy number loss	See cases	GPathogenic
Select item 147325	GRCh38/hg38 7p12.3-12.2(chr7:48876905-49055425)x1	CDC14C, LOC126860030	Copy number loss	See cases	GUncertain significance
Select item 146855	GRCh38/hg38 7p14.1-11.2(chr7:40534157-56107122)x1	ABCA13, ADCY1 +426 more	Copy number loss	See cases	GPathogenic
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	LOC121740684, LOC121740685 +4735 more	Copy number loss	See cases	GPathogenic
Select item 145645	GRCh38/hg38 7p13-12.1(chr7:44571949-53699760)x1	ABCA13, ADCY1 +200 more	Copy number loss	See cases	GPathogenic
Select item 59680	GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3	LOC129389795, LOC129389796 +636 more	Copy number gain	See cases	GPathogenic

ClinVar