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

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Search results

Items: 32

	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 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 1808407	GRCh37/hg19 16q23.1(chr16:78372847-78466128)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 1808066	GRCh37/hg19 16q23.1(chr16:78308940-78367613)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 1807996	GRCh37/hg19 16q23.1(chr16:78520848-78630819)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 1340468	GRCh37/hg19 16q23.1(chr16:78384725-78508065)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 1340402	GRCh37/hg19 16q23.1(chr16:78469169-78739257)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 980693	GRCh37/hg19 16q23.1(chr16:78229572-78687523)x1	WWOX	Copy number loss	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 980691	GRCh37/hg19 16q23.1(chr16:77928003-78594966)x4	VAT1L, CLEC3A +1 more	Copy number gain	not provided	GLikely benign
Select item 979476	GRCh37/hg19 16q23.1-23.2(chr16:78064093-79320656)x3	CLEC3A, WWOX	Copy number gain	not provided	GUncertain significance
Select item 979474	GRCh37/hg19 16q23.1(chr16:78296293-78426119)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 979472	GRCh37/hg19 16q23.1(chr16:78372597-78504169)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 815849	GRCh37/hg19 16q23.1-23.2(chr16:78426151-81049683)x3	CDYL2, CENPN +4 more	Copy number gain	not provided	GUncertain significance
Select item 815848	GRCh37/hg19 16q23.1(chr16:78420576-78519780)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 815847	GRCh37/hg19 16q23.1(chr16:78372426-78426119)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 815846	GRCh37/hg19 16q23.1(chr16:78205565-78344587)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 815845	GRCh37/hg19 16q23.1(chr16:78103821-78334723)x3	WWOX	Copy number gain	not provided	GUncertain significance
Select item 815844	GRCh37/hg19 16q23.1(chr16:77963711-78463588)x3	VAT1L, WWOX +1 more	Copy number gain	not provided	GUncertain significance
Select item 815843	GRCh37/hg19 16q23.1(chr16:77826202-78334723)x3	VAT1L, WWOX +1 more	Copy number gain	not provided	GUncertain significance
Select item 815842	GRCh37/hg19 16q23.1(chr16:77826202-78379662)x3	VAT1L, WWOX +1 more	Copy number gain	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 564355	GRCh37/hg19 16q23.1-23.2(chr16:79031223-79456467)x3	WWOX	Copy number gain	not provided	GUncertain significance
Select item 564354	GRCh37/hg19 16q23.1(chr16:78180603-78236617)x1	WWOX	Copy number loss	not provided	GUncertain significance
Select item 564353	GRCh37/hg19 16q23.1-23.2(chr16:78156871-79792370)x3	MAF, WWOX	Copy number gain	not provided	GUncertain significance
Select item 564352	GRCh37/hg19 16q23.1(chr16:77930189-78594966)x3	WWOX, CLEC3A +1 more	Copy number gain	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 564342	GRCh37/hg19 16q22.2-24.3(chr16:72515938-90155062)x3	ACSF3, ADAD2 +136 more	Copy number gain	not provided	GPathogenic

ClinVar

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Items: 32