LOC101927814[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 58085	GRCh38/hg38 16p13.11-12.1(chr16:14954894-28306843)x3	ABCC1, ABCC6 +400 more	Copy number gain	See cases	GPathogenic
Select item 151527	GRCh38/hg38 16p12.2-11.2(chr16:21350622-29202837)x3	APOBR, AQP8 +287 more	Copy number gain	See cases	GLikely pathogenic
Select item 161018	GRCh38/hg38 16p12.2(chr16:21463739-21826230)x1	IGSF6, LOC101927814 +11 more	Copy number loss	See cases	GUncertain significance
Select item 146179	GRCh38/hg38 16p12.2(chr16:21463739-21826230)x3	IGSF6, LOC101927814 +11 more	Copy number gain	See cases	GBenign
Select item 58086	GRCh38/hg38 16p12.2-11.2(chr16:21463739-29249579)x3	LOC130058727, LOC130058728 +287 more	Copy number gain	See cases	GPathogenic
Select item 145773	GRCh38/hg38 16p12.2(chr16:21483549-21851072)x3	LOC130058626, LOC130058627 +12 more	Copy number gain	See cases	GBenign
Select item 152604	GRCh38/hg38 16p12.2(chr16:21525609-21826171)x1	IGSF6, LOC101927814 +8 more	Copy number loss	See cases	GBenign
Select item 57546	GRCh38/hg38 16p12.2(chr16:21561057-21810544)x1	IGSF6, LOC101927814 +6 more	Copy number loss	See cases	GUncertain significance
Select item 151586	GRCh38/hg38 16p12.2(chr16:21585329-21717046)x1	IGSF6, LOC101927814 +6 more	Copy number loss	See cases	GBenign
Select item 147258	GRCh38/hg38 16p12.2(chr16:21588366-21826230)x3	IGSF6, LOC101927814 +6 more	Copy number gain	See cases	GBenign