LOC125146404[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58594	GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3	LOC112340388, LOC112441449 +821 more	Copy number gain	See cases	GPathogenic
Select item 150284	GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3	OR1F1, OR2C1 +916 more	Copy number gain	See cases	GPathogenic
Select item 144298	GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3	RMI2, RNF151 +842 more	Copy number gain	See cases	GPathogenic
Select item 155643	GRCh38/hg38 16p13.3-13.11(chr16:666662-15743104)x3	LOC130058340, LOC130058341 +925 more	Copy number gain	See cases	GPathogenic
Select item 144327	GRCh38/hg38 16p13.3-11.2(chr16:4644892-29170820)x3	ABAT, ABCC1 +851 more	Copy number gain	See cases	GPathogenic
Select item 155488	GRCh38/hg38 16p13.2-13.13(chr16:9992260-10429871)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	GUncertain significance
Select item 155219	GRCh38/hg38 16p13.2-13.13(chr16:9992260-10427239)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	GUncertain significance
Select item 155073	GRCh38/hg38 16p13.2-13.13(chr16:9992260-10445959)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	GUncertain significance
Select item 154243	GRCh38/hg38 16p13.2(chr16:9992260-10398815)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	GLikely benign
Select item 151406	GRCh38/hg38 16p13.2-13.13(chr16:9992260-10429970)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 152697	GRCh38/hg38 16p13.2-13.13(chr16:9998191-10426437)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	GUncertain significance
Select item 154562	GRCh38/hg38 16p13.2-13.13(chr16:10012281-10426437)x3	ATF7IP2, GRIN2A +14 more	Copy number gain	See cases	GUncertain significance