Related gene-specific medical variations for Gene (Select 200150) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809364	GRCh37/hg19 1q43(chr1:242534486-242646475)x1	PLD5	Copy number loss	not provided	GUncertain significance
Select item 1807890	GRCh37/hg19 1q43(chr1:242403224-242512725)x1	PLD5	Copy number loss	not provided	GUncertain significance
Select item 814190	GRCh37/hg19 1q43(chr1:242200571-242466974)x1	PLD5	Copy number loss	not provided	GUncertain significance
Select item 638140	GRCh37/hg19 1q43(chr1:242292690-243094146)x4	PLD5	Copy number gain	See cases	GLikely benign
Select item 442179	GRCh37/hg19 1q43(chr1:242401835-243027981)x1	PLD5	Copy number loss	See cases	GLikely benign
Select item 221688	GRCh38/hg38 1q43(chr1:242366167-242391262)x1	PLD5	Copy number loss	Premature ovarian failure	GBenign

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