"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 2685756	GRCh37/hg19 Xq21.31(chrX:90757308-91142616)x2	PCDH11X	Copy number gain	not provided	GUncertain significance
Select item 2685715	GRCh37/hg19 Xq21.31-25(chrX:91274467-126799984)x1	ACSL4, AGTR2 +175 more	Copy number loss	not provided	GPathogenic
Select item 2684999	GRCh37/hg19 Xq21.31-21.32(chrX:91590732-92949806)x3	FAM133A, NAP1L3 +1 more	Copy number gain	not provided	GUncertain significance
Select item 2684998	GRCh37/hg19 Xq21.31(chrX:90625130-91373172)x3	PABPC5, PCDH11X	Copy number gain	not provided	GUncertain significance
Select item 2684996	GRCh37/hg19 Xq21.1-24(chrX:77212972-118576590)x3	ACSL4, AGTR2 +159 more	Copy number gain	not provided	GPathogenic
Select item 1809472	GRCh37/hg19 Xq21.31(chrX:90036297-91527166)x3	PABPC5, PCDH11X	Copy number gain	not provided	GUncertain significance
Select item 1808201	GRCh37/hg19 Xq21.31-21.33(chrX:87082472-95826084)x3	CPXCR1, FAM133A +4 more	Copy number gain	not provided	GUncertain significance
Select item 1808153	GRCh37/hg19 Xq21.31(chrX:90926834-91135064)x2	PCDH11X	Copy number gain	not provided	GUncertain significance
Select item 1341233	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	RADX, RAI2 +818 more	Copy number loss	not provided	GPathogenic
Select item 1341223	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	GPM6B, KLHL15 +818 more	Copy number gain	not provided	GPathogenic
Select item 1340863	GRCh37/hg19 Xq21.31(chrX:90943434-91397723)x3	PCDH11X	Copy number gain	not provided	GUncertain significance
Select item 979829	GRCh37/hg19 Xq21.1-25(chrX:77514079-127770854)x1	ACSL4, ACTRT1 +201 more	Copy number loss	not provided	GPathogenic
Select item 816368	GRCh37/hg19 Xq21.1-28(chrX:84387417-155233731)x1	ABCD1, ACSL4 +398 more	Copy number loss	not provided	GPathogenic
Select item 816364	GRCh37/hg19 Xq21.1-28(chrX:78444738-155233731)x1	ABCD1, ACSL4 +410 more	Copy number loss	not provided	GPathogenic
Select item 564870	GRCh37/hg19 Xq21.31(chrX:91281524-91385275)x0	PCDH11X	Copy number loss	not provided	GUncertain significance
Select item 564869	GRCh37/hg19 Xq21.31(chrX:91166156-91737877)x0	PCDH11X	Copy number loss	not provided	GUncertain significance
Select item 564868	GRCh37/hg19 Xq21.31-28(chrX:91140025-155233731)x1	ABCD1, ACSL4 +390 more	Copy number loss	not provided	GPathogenic
Select item 564867	GRCh37/hg19 Xq21.31-21.33(chrX:91023672-97733935)x1	RPA4, NAP1L3 +3 more	Copy number loss	not provided	GUncertain significance
Select item 564866	GRCh37/hg19 Xq21.31-21.33(chrX:86794810-96275443)x1	NAP1L3, DIAPH2 +7 more	Copy number loss	not provided	GPathogenic