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

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Search results

Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685218	GRCh37/hg19 6q26(chr6:162771917-162875706)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 2685217	GRCh37/hg19 6q26(chr6:162686408-162912388)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 2685216	GRCh37/hg19 6q26(chr6:162442896-162716261)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 2684461	GRCh37/hg19 6q26(chr6:162358262-162702832)x3	PRKN	Copy number gain	not provided	GUncertain significance
Select item 1340945	GRCh37/hg19 6q26(chr6:162841880-162982289)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 1340909	GRCh37/hg19 6q26(chr6:162813663-162928416)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 1340638	GRCh37/hg19 6q26(chr6:162802027-162990128)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 1340386	GRCh37/hg19 6q26(chr6:162672821-162958851)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 1340069	GRCh37/hg19 6q26(chr6:162672820-163007394)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 979591	GRCh37/hg19 6q26(chr6:161593323-161814295)x3	AGPAT4, PRKN	Copy number gain	not provided	GUncertain significance
Select item 979590	GRCh37/hg19 6q26(chr6:162442895-162966685)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 979586	GRCh37/hg19 6q26(chr6:162434342-162551099)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 979585	GRCh37/hg19 6q26(chr6:162369855-162680559)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 979584	GRCh37/hg19 6q26(chr6:162212864-162530432)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 979583	GRCh37/hg19 6q26(chr6:162854370-162940238)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 979582	GRCh37/hg19 6q26(chr6:162680773-163427383)x1	PRKN, PACRG	Copy number loss	not provided	GLikely benign
Select item 814903	GRCh37/hg19 6q26(chr6:162765163-163266877)x3	PACRG, PRKN	Copy number gain	not provided	GUncertain significance
Select item 814902	GRCh37/hg19 6q26(chr6:162673130-163007394)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 814901	GRCh37/hg19 6q26-27(chr6:162661108-170919482)x1	CEP43, DACT2 +33 more	Copy number loss	not provided	GPathogenic
Select item 814900	GRCh37/hg19 6q26(chr6:162542083-162802027)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 814899	GRCh37/hg19 6q26(chr6:162513435-162799405)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 814898	GRCh37/hg19 6q26(chr6:162496034-162770009)x3	PRKN	Copy number gain	not provided	GUncertain significance
Select item 814897	GRCh37/hg19 6q26-27(chr6:162452035-170919482)x1	GPR31, KIF25 +33 more	Copy number loss	not provided	GPathogenic
Select item 814896	GRCh37/hg19 6q26(chr6:162422242-162643440)x3	PRKN	Copy number gain	not provided	GUncertain significance
Select item 814895	GRCh37/hg19 6q26(chr6:162203626-162305145)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 814894	GRCh37/hg19 6q26(chr6:162178475-162289828)x1	PRKN	Copy number loss	not provided	GLikely benign
Select item 814893	GRCh37/hg19 6q26(chr6:162125751-162347138)x1	PRKN	Copy number loss	not provided	GLikely benign
Select item 814892	GRCh37/hg19 6q26(chr6:162064527-162456523)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 814891	GRCh37/hg19 6q26(chr6:161963572-162131676)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 814890	GRCh37/hg19 6q26(chr6:161836241-162000352)x1	PRKN	Copy number loss	not provided	GLikely benign
Select item 563254	GRCh37/hg19 6q26(chr6:162838224-163036171)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 563253	GRCh37/hg19 6q26(chr6:162745744-163117879)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 563252	GRCh37/hg19 6q26(chr6:162693562-163399349)x3	PRKN, PACRG	Copy number gain	not provided	GUncertain significance
Select item 563251	GRCh37/hg19 6q26(chr6:162573253-162693547)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 563250	GRCh37/hg19 6q26(chr6:162545871-163112949)x3	PRKN	Copy number gain	not provided	GUncertain significance
Select item 563249	GRCh37/hg19 6q26(chr6:162341941-162408937)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 563248	GRCh37/hg19 6q26(chr6:162335175-162612003)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 563247	GRCh37/hg19 6q26(chr6:162283948-162735264)x1	PRKN	Copy number loss	not provided	GUncertain significance
Select item 563246	GRCh37/hg19 6q25.3-26(chr6:160524800-161855470)x3	SLC22A3, SLC22A2 +7 more	Copy number gain	not provided	GUncertain significance
Select item 563245	GRCh37/hg19 6q25.3-27(chr6:159844762-170919482)x3	ACAT2, AFDN +49 more	Copy number gain	not provided	GPathogenic

ClinVar

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Germline classification

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Molecular consequence

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Items: 40