Hs03866105_cn

• Gene Symbol: LHFP
• Assay Reference Genome Location: Chr.13:39360849 on build GRCh38
• Cytoband: 13q13.3

Target Gene Details

• Entrez Gene ID: 10186
• Gene Name: lipoma HMGIC fusion partner
• Gene Aliases: -
• Location: Chr.13:39342892-39603219 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LHFP	NM_005780.2			NP_005771.1
	XM_011534861.1			XP_011533163.1
	AF098807.1			AAD31386.1
	AK129819.1
	AK223369.1			BAD97089.1
	AK313036.1
	BC017824.1			AAH17824.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv3249274	Chr.13:39360298 - 39361595 on Build GRCh38	Deletion	LHFP
nsv511518	Chr.13:39359940 - 39362766 on Build GRCh38	Loss	LHFP
nsv1036674	Chr.13:39267345 - 39433980 on Build GRCh38	Loss	LHFP
esv2747287	Chr.13:39359973 - 39361527 on Build GRCh38	Deletion	LHFP
nsv561535	Chr.13:39360432 - 39361013 on Build GRCh38	Gain	LHFP
esv1008099	Chr.13:39360252 - 39361396 on Build GRCh38	Loss	LHFP
esv995533	Chr.13:39360357 - 39360868 on Build GRCh38	Loss	LHFP
dgv103e215	Chr.13:39359999 - 39361470 on Build GRCh38	Deletion	LHFP
nsv820588	Chr.13:39359954 - 39361396 on Build GRCh38	Deletion	LHFP
nsv512313	Chr.13:39359967 - 39361409 on Build GRCh38	Loss	LHFP
nsv820008	Chr.13:39359864 - 39361437 on Build GRCh38	Loss	LHFP
nsv1054600	Chr.13:39227146 - 39970890 on Build GRCh38	Gain	MIR4305 COG6 LHFP
nsv64628	Chr.13:39360082 - 39361378 on Build GRCh38	Deletion	LHFP
esv996813	Chr.13:39355568 - 39362933 on Build GRCh38	Deletion	LHFP
nsv1069512	Chr.13:39360062 - 39361363 on Build GRCh38	Deletion	LHFP
esv1412441	Chr.13:39360051 - 39361349 on Build GRCh38	Deletion	LHFP
dgv51n73	Chr.13:39360064 - 39361380 on Build GRCh38	Deletion	LHFP
esv3631831	Chr.13:39360099 - 39361415 on Build GRCh38	Loss	LHFP
nsv561533	Chr.13:39360381 - 39361013 on Build GRCh38	Gain+Loss	LHFP
dgv958n106	Chr.13:39360045 - 39361376 on Build GRCh38	Deletion	LHFP
esv25053	Chr.13:39359490 - 39361250 on Build GRCh38	Gain+Loss	LHFP
esv988930	Chr.13:39360046 - 39361343 on Build GRCh38	Deletion	LHFP
nsv1152038	Chr.13:39360047 - 39361401 on Build GRCh38	Deletion	LHFP

More Information

Additional Information:

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation, Validated

Gene Ontology Categories:

Function(s)

DNA binding