LOC130057832[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic
Select item 154952	GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	LOC116268473, LOC116268474 +1244 more	Copy number gain	See cases	GPathogenic
Select item 147691	GRCh38/hg38 15q25.2-26.3(chr15:82859676-101810992)x3	LOC130057943, LOC130057944 +664 more	Copy number gain	See cases	GPathogenic
Select item 146595	GRCh38/hg38 15q25.2-26.3(chr15:83711377-101843270)x3	LOC130057907, LOC130057908 +630 more	Copy number gain	See cases	GPathogenic
Select item 58580	GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3	ABHD2, ACAN +611 more	Copy number gain	See cases	GPathogenic
Select item 58379	GRCh38/hg38 15q25.3(chr15:85185563-85639683)x3	AKAP13, LOC112272622 +29 more	Copy number gain	See cases	GUncertain significance
Select item 151927	GRCh38/hg38 15q25.3(chr15:85228050-85544770)x3	AKAP13, LOC112272622 +21 more	Copy number gain	See cases	GLikely benign
Select item 145300	GRCh38/hg38 15q25.3(chr15:85228050-85593726)x3	AKAP13, LOC112272622 +23 more	Copy number gain	See cases	GBenign
Select item 145718	GRCh38/hg38 15q25.3(chr15:85290841-85544770)x3	AKAP13, LOC112272622 +20 more	Copy number gain	See cases	GBenign
Select item 58381	GRCh38/hg38 15q25.3(chr15:85327915-85556913)x3	AKAP13, LOC112272622 +16 more	Copy number gain	See cases	GUncertain significance