LINC01943[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	HAAO, HADHA +2457 more	Copy number gain	See cases	GBenign
Select item 145403	GRCh38/hg38 2p12-11.2(chr2:77025216-90282666)x3	ATOH8, C2orf68 +302 more	Copy number gain	See cases	GPathogenic
Select item 153632	GRCh38/hg38 2p11.2(chr2:85014686-88826619)x1	ATOH8, C2orf68 +179 more	Copy number loss	See cases	GPathogenic
Select item 59790	GRCh38/hg38 2p11.2(chr2:86797744-87705899)x3	CD8A, CD8B +14 more	Copy number gain	See cases	GBenign
Select item 150013	GRCh38/hg38 2p11.2(chr2:87068547-87705910)x1	CYTOR, LINC01943 +8 more	Copy number loss	See cases	GLikely benign
Select item 147277	GRCh38/hg38 2p11.2(chr2:87098178-87705899)x3	CYTOR, LINC01943 +4 more	Copy number gain	See cases	GBenign
Select item 146363	GRCh38/hg38 2p11.2-11.1(chr2:87098178-91884275)x3	LOC122787150, LOC122787151 +104 more	Copy number gain	See cases	GUncertain significance
Select item 144698	GRCh38/hg38 2p11.2(chr2:87098204-87705910)x1	CYTOR, LINC01943 +4 more	Copy number loss	See cases	GBenign/Likely benign
Select item 144695	GRCh38/hg38 2p11.2(chr2:87098204-87705910)x3	CYTOR, LINC01943 +4 more	Copy number gain	See cases	GBenign
Select item 145392	GRCh38/hg38 2p11.2(chr2:87148950-87705910)x1	CYTOR, LINC01943 +4 more	Copy number loss	See cases	GLikely benign
Select item 145391	GRCh38/hg38 2p11.2(chr2:87148950-87705910)x3	CYTOR, LINC01943 +4 more	Copy number gain	See cases	GBenign/Likely benign
Select item 161013	GRCh38/hg38 2p11.2(chr2:87148954-87705899)x1	CYTOR, LINC01943 +4 more	Copy number loss	See cases	GBenign
Select item 147889	GRCh38/hg38 2p11.2(chr2:87148954-87655401)x1	CYTOR, LINC01943 +4 more	Copy number loss	See cases	GBenign
Select item 147888	GRCh38/hg38 2p11.2(chr2:87148954-87655401)x3	CYTOR, LINC01943 +4 more	Copy number gain	See cases	GConflicting classifications of pathogenicity
Select item 146182	GRCh38/hg38 2p11.2(chr2:87148954-87705899)x3	CYTOR, LINC01943 +4 more	Copy number gain	See cases	GConflicting classifications of pathogenicity
Select item 144358	GRCh38/hg38 2p11.2(chr2:87148954-87961277)x3	CYTOR, LINC01943 +6 more	Copy number gain	See cases	GBenign
Select item 33823	GRCh38/hg38 2p11.2(chr2:87148954-87705899)x1	CYTOR, LINC01943 +4 more	Copy number loss	See cases	GBenign
Select item 148476	GRCh38/hg38 2p11.2(chr2:87375475-90282666)x3	CYTOR, EIF2AK3 +101 more	Copy number gain	See cases	GUncertain significance
Select item 149404	GRCh38/hg38 2p11.2(chr2:87453471-87583817)x1	CYTOR, LINC01943 +1 more	Copy number loss	See cases	GLikely benign