ClinVar for Gene (Select 123493308) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1278187	NM_021147.5(CCNO):c.-65G>T	CCNO, LOC123493308	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1275363	NC_000005.10:g.55233776G>A	CCNO, LOC123493308	Single nucleotide variant	not provided	GBenign
Select item 1272415	NC_000005.10:g.55233802A>C	CCNO, LOC123493308	Single nucleotide variant	not provided	GBenign
Select item 1263712	NC_000005.10:g.55233630C>G	CCNO, LOC123493308	Single nucleotide variant	not provided	GBenign
Select item 1221093	NC_000005.10:g.55233874GTCACTGCGGAGCCCGG[1]	CCNO, LOC123493308	Microsatellite	not provided	GBenign
Select item 150391	GRCh38/hg38 5q11.2(chr5:55028257-55939697)x3	CCNO, CCNO-DT +35 more	Copy number gain	See cases	GUncertain significance
Select item 149824	GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3	ACTBL2, ADAMTS12 +1445 more	Copy number gain	See cases	GPathogenic
Select item 148959	GRCh38/hg38 5p12-q11.2(chr5:45566861-56506493)x3	ANKRD55, ARL15 +125 more	Copy number gain	See cases	GUncertain significance
Select item 148227	GRCh38/hg38 5p13.2-q12.1(chr5:35201559-61903141)x3	LINC02057, LINC02101 +518 more	Copy number gain	See cases	GPathogenic
Select item 59608	GRCh38/hg38 5q11.1-11.2(chr5:50462100-55862985)x1	ARL15, CCNO +96 more	Copy number loss	See cases	GPathogenic
Select item 57149	GRCh38/hg38 5q11.1-12.1(chr5:50288355-63149770)x1	ACTBL2, ANKRD55 +269 more	Copy number loss	See cases	GPathogenic