LINC03003[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	CYP39A1, DAAM2 +2577 more	Copy number gain	See cases	GPathogenic
Select item 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	LOC129995913, LOC129995914 +1340 more	Copy number gain	See cases	GPathogenic
Select item 153490	GRCh38/hg38 6p22.1(chr6:28763187-29769828)x3	GABBR1, HCG14 +61 more	Copy number gain	See cases	GUncertain significance
Select item 149276	GRCh38/hg38 6p22.1(chr6:28954915-29358240)x1	HCG15, HCG16 +18 more	Copy number loss	See cases	GLikely benign
Select item 150190	GRCh38/hg38 6p22.1(chr6:28954920-29358310)x3	HCG15, HCG16 +18 more	Copy number gain	See cases	GLikely benign

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