ClinVar (all) for Orgtrack (Select 505287) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 147989	GRCh38/hg38 17q21.31(chr17:46347056-46661960)x1	ARL17A, ARL17B +4 more	Copy number loss	See cases	GBenign
Select item 147988	GRCh38/hg38 6p25.3(chr6:265879-350944)x1	DUSP22, LOC126859546 +23 more	Copy number loss	See cases	GBenign
Select item 147987	GRCh38/hg38 17p11.2(chr17:19031266-19148137)x1	GRAP, GRAPL +6 more	Copy number loss	See cases	GBenign
Select item 147986	GRCh38/hg38 17q21.31(chr17:46304332-46685375)x3	ARL17A, ARL17B +5 more	Copy number gain	See cases	GBenign
Select item 147980	GRCh37/hg19 22q11.23(chr22:24371005-24382415)x0	GSTT1, GSTT1-AS1 +1 more	Copy number loss	See cases	GBenign
Select item 147978	GRCh38/hg38 17q12(chr17:36379367-36387940)x1	TBC1D3H	Copy number loss	See cases	GBenign
Select item 147977	GRCh38/hg38 10q26.3(chr10:133453852-133539242)x3	CYP2E1, LOC110599585 +5 more	Copy number gain	See cases	GBenign
Select item 146640	GRCh38/hg38 22q11.21(chr22:18339130-21003834)x3	AIFM3, ARVCF +179 more	Copy number gain	See cases	GPathogenic
Select item 146639	GRCh38/hg38 14q32.33(chr14:105023396-106850750)x1	BRF1, BTBD6 +174 more	Copy number loss	See cases	GPathogenic
Select item 146638	GRCh38/hg38 14q32.12-32.33(chr14:92540983-104863658)x3	ZFYVE21, ZNF839 +662 more	Copy number gain	See cases	GPathogenic
Select item 146637	GRCh38/hg38 Xp22.33-22.2(chrX:2936461-17287323)x2	ACE2, ACE2-DT +262 more	Copy number gain	See cases	GPathogenic
Select item 146636	GRCh38/hg38 18p11.32-11.31(chr18:131500-4421014)x3	ADCYAP1, CETN1 +119 more	Copy number gain	See cases	GPathogenic
Select item 146635	GRCh38/hg38 4q35.1-35.2(chr4:186187749-189800953)x1	MTNR1A, TRIML1 +62 more	Copy number loss	See cases	GPathogenic
Select item 146634	GRCh38/hg38 15q11.2-13.1(chr15:23462105-28290061)x1	ATP10A, ATP10A-DT +140 more	Copy number loss	See cases	GPathogenic
Select item 146623	GRCh38/hg38 14q22.1-22.3(chr14:51544846-55320598)x1	BMP4, CDKN3 +147 more	Copy number loss	See cases	GPathogenic
Select item 146622	GRCh38/hg38 Yq11.221-12(chrY:15631816-57211010)x0	BPY2, BPY2B +65 more	Copy number loss	See cases	GPathogenic
Select item 146621	GRCh38/hg38 Xq27.1-28(chrX:140783390-155611114)x2	AVPR2, BCAP31 +393 more	Copy number gain	See cases	GPathogenic