"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684820	GRCh37/hg19 16q23.1(chr16:77075284-78151019)x3	ADAMTS18, CLEC3A +5 more	Copy number gain	not provided	GUncertain significance
Select item 2684818	GRCh37/hg19 16q23.1(chr16:76969076-78821137)x3	ADAMTS18, CLEC3A +5 more	Copy number gain	not provided	GUncertain significance
Select item 2684813	GRCh37/hg19 16q22.1-23.2(chr16:70607067-81561138)x3	ADAMTS18, ADAT1 +67 more	Copy number gain	not provided	GPathogenic
Select item 1809453	GRCh37/hg19 16q23.1(chr16:76472469-77366668)x3	ADAMTS18, CNTNAP4 +2 more	Copy number gain	not provided	GUncertain significance
Select item 1809401	GRCh37/hg19 16q22.3-23.1(chr16:73673334-78137887)x1	ADAMTS18, ADAT1 +29 more	Copy number loss	not provided	GUncertain significance
Select item 1808954	GRCh37/hg19 16q23.1(chr16:77127830-79168848)x3	ADAMTS18, CLEC3A +5 more	Copy number gain	not provided	GUncertain significance
Select item 1807975	GRCh37/hg19 16q23.1(chr16:77320515-77463907)x1	ADAMTS18	Copy number loss	not provided	GUncertain significance
Select item 1807619	GRCh37/hg19 16q23.1(chr16:77323050-77931019)x3	ADAMTS18, NUDT7 +1 more	Copy number gain	not provided	GUncertain significance
Select item 980692	GRCh37/hg19 16q23.1(chr16:77451482-78341924)x3	CLEC3A, VAT1L +3 more	Copy number gain	not provided	GUncertain significance
Select item 815841	GRCh37/hg19 16q23.1(chr16:77323049-77698037)x3	ADAMTS18	Copy number gain	not provided	GUncertain significance
Select item 815840	GRCh37/hg19 16q23.1(chr16:77268506-77320605)x1	ADAMTS18	Copy number loss	not provided	GUncertain significance
Select item 815839	GRCh37/hg19 16q23.1(chr16:77191839-77856232)x1	MON1B, ADAMTS18 +3 more	Copy number loss	not provided	GUncertain significance
Select item 815838	GRCh37/hg19 16q23.1(chr16:77112563-79015106)x3	CLEC3A, WWOX +5 more	Copy number gain	not provided	GUncertain significance
Select item 815837	GRCh37/hg19 16q23.1(chr16:77004778-77672338)x3	ADAMTS18, SYCE1L +1 more	Copy number gain	not provided	GUncertain significance
Select item 564350	GRCh37/hg19 16q23.1(chr16:77318570-77469711)x1	ADAMTS18	Copy number loss	not provided	GUncertain significance
Select item 564349	GRCh37/hg19 16q23.1(chr16:77087399-78395997)x3	ADAMTS18, MON1B +5 more	Copy number gain	not provided	GUncertain significance
Select item 564348	GRCh37/hg19 16q23.1(chr16:76955286-79080596)x3	MON1B, VAT1L +5 more	Copy number gain	not provided	GUncertain significance
Select item 564347	GRCh37/hg19 16q23.1(chr16:76472468-77369927)x3	CNTNAP4, MON1B +2 more	Copy number gain	not provided	GUncertain significance
Select item 564342	GRCh37/hg19 16q22.2-24.3(chr16:72515938-90155062)x3	ACSF3, ADAD2 +136 more	Copy number gain	not provided	GPathogenic