RNVU1-18[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57409	GRCh38/hg38 1p11.2-q22(chr1:120836007-149583533)x3	BCL9, LINC00623 +213 more	Copy number gain	See cases	GPathogenic
Select item 145983	GRCh38/hg38 1p13.2-11.2(chr1:121086594-144935242)x3	FAM72B, FAM72C +42 more	Copy number gain	See cases	GPathogenic
Select item 58087	GRCh38/hg38 1p12-q21.2(chr1:121086594-144935242)x3	FAM72B, FAM72C +42 more	Copy number gain	See cases	GPathogenic
Select item 153061	GRCh38/hg38 1q21.1-21.2(chr1:143515074-149076087)x1	ACP6, ANKRD34A +178 more	Copy number loss	See cases	GPathogenic
Select item 150976	GRCh38/hg38 1q21.1-21.2(chr1:143515074-149563337)x1	LOC129931352, LOC129931353 +183 more	Copy number loss	See cases	GPathogenic
Select item 148361	GRCh38/hg38 1q21.1-21.2(chr1:143515074-149076087)x1	ACP6, ANKRD34A +179 more	Copy number loss	See cases	GPathogenic
Select item 147710	GRCh38/hg38 1q21.1-21.2(chr1:143515074-149076087)x3	ACP6, ANKRD34A +178 more	Copy number gain	See cases	GPathogenic
Select item 146706	GRCh38/hg38 1q21.1-21.2(chr1:143515074-144625016)x1	FAM72C, H3-7 +25 more	Copy number loss	See cases	GBenign
Select item 58491	GRCh38/hg38 1q21.1-21.2(chr1:143515074-149076087)x1	LOC126805854, LOC128071544 +179 more	Copy number loss	See cases	GPathogenic
Select item 150940	GRCh38/hg38 1q21.1(chr1:143545534-143749316)x3	LOC107985108, RNVU1-17 +4 more	Copy number gain	See cases	GLikely benign
Select item 154717	GRCh38/hg38 1q21.1(chr1:143546346-143780484)x1	LOC107985108, RNVU1-17 +4 more	Copy number loss	See cases	GBenign
Select item 148173	GRCh38/hg38 1q21.1(chr1:143546346-143737831)x1	LOC107985108, RNVU1-17 +4 more	Copy number loss	See cases	GBenign
Select item 148172	GRCh38/hg38 1q21.1(chr1:143546346-143737831)x3	LOC107985108, RNVU1-17 +4 more	Copy number gain	See cases	GBenign
Select item 150006	GRCh38/hg38 1q21.1(chr1:143546356-143737826)x1	LOC107985108, RNVU1-17 +4 more	Copy number loss	See cases	GLikely benign
Select item 147251	GRCh38/hg38 1q21.1(chr1:143546375-143780462)x1	LOC107985108, RNVU1-17 +4 more	Copy number loss	See cases	GBenign