"ISCA site 4"[submitter] AND "TARS3"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144251	GRCh38/hg38 15q26.1-26.3(chr15:93198717-101843270)x1	LYSMD4, MCTP2 +224 more	Copy number loss	See cases	GPathogenic
Select item 57195	GRCh38/hg38 15q26.2-26.3(chr15:94033008-101843270)x3	ADAMTS17, ALDH1A3 +218 more	Copy number gain	See cases	GPathogenic
Select item 149341	GRCh38/hg38 15q26.3(chr15:101395560-101843276)x3	LINC02348, LOC121847966 +15 more	Copy number gain	See cases	GLikely benign
Select item 144538	GRCh38/hg38 15q26.3(chr15:101500643-101716531)x3	LINC02348, LOC126862257 +6 more	Copy number gain	See cases	GBenign
Select item 150059	GRCh38/hg38 15q26.3(chr15:101608448-101716531)x3	LINC02348, LOC130058078 +4 more	Copy number gain	See cases	GLikely benign
Select item 144300	GRCh38/hg38 15q26.3(chr15:101621277-101666176)x3	LOC130058078, LOC130058079 +3 more	Copy number gain	See cases	GBenign
Select item 144266	GRCh38/hg38 15q26.3(chr15:101621277-101708810)x3	LOC130058078, LOC130058079 +3 more	Copy number gain	See cases	GBenign
Select item 144573	GRCh38/hg38 15q26.3(chr15:101621303-101711860)x3	LOC130058078, LOC130058079 +3 more	Copy number gain	See cases	GBenign/Likely benign
Select item 57191	GRCh38/hg38 15q26.3(chr15:101642152-101843270)x3	LOC126862258, LOC126862259 +8 more	Copy number gain	See cases	GBenign
Select item 57055	GRCh38/hg38 15q26.3(chr15:101666117-101723215)x3	TARS3	Copy number gain	See cases	GBenign
Select item 150725	GRCh38/hg38 15q26.3(chr15:101685919-101843276)x1	LOC126862258, LOC126862259 +5 more	Copy number loss	See cases	GLikely benign
Select item 147947	GRCh38/hg38 15q26.3(chr15:101686039-101723215)x3	TARS3	Copy number gain	See cases	GConflicting classifications of pathogenicity