LINC01202[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58118	GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3	LOC132089226, LOC132089227 +1167 more	Copy number gain	See cases	GPathogenic
Select item 149231	GRCh38/hg38 5q33.1-34(chr5:152443869-166104392)x1	ADAM19, ADRA1B +295 more	Copy number loss	See cases	GPathogenic
Select item 58390	GRCh38/hg38 5q33.1-34(chr5:152761187-167248053)x1	ADAM19, ADRA1B +280 more	Copy number loss	See cases	GPathogenic
Select item 144365	GRCh38/hg38 5q33.3-35.3(chr5:156825512-181269805)x3	LOC129995440, LOC129995441 +864 more	Copy number gain	See cases	GPathogenic
Select item 1707452	Single allele	ADRA1B, ATP10B +111 more	Duplication	not specified	GUncertain significance
Select item 149967	GRCh38/hg38 5q33.3-34(chr5:158941354-164386760)x1	GABRA1, GABRA6 +108 more	Copy number loss	See cases	GPathogenic
Select item 2499664	GRCh38/hg38 5q34(chr5:161615157-162040104)	GABRA1, GABRA6 +2 more	Copy number loss	See cases	GUncertain significance
Select item 3341136	NC_000005.10:g.161832946_162532555del	GABRA1, GABRG2 +1 more	Deletion	not provided	GPathogenic
Select item 58393	GRCh38/hg38 5q34(chr5:161909955-164086917)x1	CCNG1, GABRG2 +17 more	Copy number loss	See cases	GPathogenic
Select item 148444	GRCh38/hg38 5q34(chr5:161925019-162133217)x3	GABRG2, LINC01202	Copy number gain	See cases	GUncertain significance
Select item 153230	GRCh38/hg38 5q34(chr5:161954028-162107018)x1	GABRG2, LINC01202	Copy number loss	See cases	GPathogenic