"GeneDx"[submitter] AND "LOC130001435"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58437	GRCh38/hg38 9p24.3(chr9:52389-356138)x3	DOCK8, DOCK8-AS1 +16 more	Copy number gain	See cases	GUncertain significance
Select item 152051	GRCh38/hg38 9p24.3(chr9:62525-386070)x3	DOCK8, DOCK8-AS1 +16 more	Copy number gain	See cases	GLikely benign
Select item 144972	GRCh38/hg38 9p24.3(chr9:163131-271257)x3	DOCK8, DOCK8-AS1 +5 more	Copy number gain	See cases	GBenign
Select item 145917	GRCh38/hg38 9p24.3(chr9:185579-288161)x4	DOCK8, DOCK8-AS1 +7 more	Copy number gain	See cases	GLikely benign
Select item 151952	GRCh38/hg38 9p24.3(chr9:211086-314969)x3	DOCK8, DOCK8-AS1 +7 more	Copy number gain	See cases	GBenign
Select item 145922	GRCh38/hg38 9p24.3(chr9:211086-271257)x3	DOCK8, DOCK8-AS1 +4 more	Copy number gain	See cases	GLikely benign
Select item 59047	GRCh38/hg38 9p24.3(chr9:211086-274576)x1	DOCK8, DOCK8-AS1 +4 more	Copy number loss	See cases	GUncertain significance
Select item 1187835	NC_000009.12:g.214679G>A	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 1224206	NC_000009.12:g.214706G>C	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1220363	NC_000009.12:g.214719C>T	DOCK8-AS1, LOC130001435 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 674418	NM_203447.3(DOCK8):c.-173A>G	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not specified +1 more	GBenign
Select item 1321799	NC_000009.12:g.214847A>C	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 369626	NM_203447.3(DOCK8):c.-113C>T	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not provided +2 more	GBenign