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

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809424	GRCh37/hg19 15q24.3-26.3(chr15:77512817-102035027)x3	ABHD17C, ABHD2 +139 more	Copy number gain	not provided	GPathogenic
Select item 1341270	GRCh37/hg19 15q26.3(chr15:99490397-99521812)x1	IGF1R, PGPEP1L	Copy number loss	not provided	GLikely pathogenic
Select item 980652	GRCh37/hg19 15q26.3(chr15:99428748-99762146)x3	PGPEP1L, IGF1R +2 more	Copy number gain	not provided	GUncertain significance
Select item 980650	GRCh37/hg19 15q26.3(chr15:99408416-99877293)x3	SYNM, TTC23 +3 more	Copy number gain	not provided	GUncertain significance
Select item 980643	GRCh37/hg19 15q26.2-26.3(chr15:98275761-102358202)x1	ALDH1A3, SYNM +19 more	Copy number loss	not provided	GPathogenic
Select item 815760	GRCh37/hg19 15q26.3(chr15:99467707-99507214)x1	IGF1R	Copy number loss	not provided	GLikely pathogenic
Select item 815759	GRCh37/hg19 15q26.3(chr15:99459795-100032533)x3	LRRC28, PGPEP1L +3 more	Copy number gain	not provided	GUncertain significance
Select item 815758	GRCh37/hg19 15q26.3(chr15:99212378-99653800)x3	PGPEP1L, IGF1R +1 more	Copy number gain	not provided	GUncertain significance
Select item 815757	GRCh37/hg19 15q26.3(chr15:98982492-99411100)x1	IGF1R	Copy number loss	not provided	GLikely pathogenic
Select item 815756	GRCh37/hg19 15q26.3(chr15:98806822-100262828)x3	PGPEP1L, MEF2A +4 more	Copy number gain	not provided	GUncertain significance
Select item 815755	GRCh37/hg19 15q26.3(chr15:98795669-102429112)x1	OR4F15, PGPEP1L +19 more	Copy number loss	not provided	GPathogenic
Select item 815754	GRCh37/hg19 15q26.3(chr15:98686212-102429112)x1	SYNM, CHSY1 +19 more	Copy number loss	not provided	GPathogenic
Select item 815743	GRCh37/hg19 15q25.3-26.3(chr15:87189245-102429112)x1	ABHD2, ACAN +76 more	Copy number loss	not provided	GPathogenic
Select item 564234	GRCh37/hg19 15q26.3(chr15:99350059-100112556)x3	PGPEP1L, MEF2A +4 more	Copy number gain	not provided	GUncertain significance
Select item 564233	GRCh37/hg19 15q26.3(chr15:99198450-99913428)x3	IGF1R, LRRC28 +3 more	Copy number gain	not provided	GUncertain significance
Select item 564232	GRCh37/hg19 15q26.2-26.3(chr15:98144229-99857338)x1	PGPEP1L, ARRDC4 +4 more	Copy number loss	not provided	GLikely pathogenic
Select item 564229	GRCh37/hg19 15q26.1-26.3(chr15:89743929-102429112)x3	ABHD2, ADAMTS17 +66 more	Copy number gain	not provided	GPathogenic
Select item 564221	GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3	ABHD17C, ABHD2 +143 more	Copy number gain	not provided	GPathogenic
Select item 564214	GRCh37/hg19 15q23-26.3(chr15:71329220-102270758)x3	ABHD17C, ABHD2 +215 more	Copy number gain	not provided	GPathogenic