Hs02828944_cn

• Gene Symbol: RP9P
• Assay Reference Genome Location: Chr.7:32921755 on build GRCh38
• Cytoband: 7p14.3

Target Gene Details

• Entrez Gene ID: 441212
• Gene Name: retinitis pigmentosa 9 pseudogene
• Gene Aliases: -
• Location: Chr.7:32916815-32943170 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
RP9P	NR_003500.1
	AF274938.1			AAK07516.1
	AK091223.1	3	3096

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1029220	Chr.7:32881872 - 33222578 on Build GRCh38	Gain	NT5C3A KBTBD2 RP9P FKBP9 BBS9 RP9
dgv1080e201	Chr.7:32621750 - 35008557 on Build GRCh38	Deletion	DPY19L1P1 MIR550A2 NT5C3A KBTBD2 LOC100421336 FKBP9 LINC00997 BMPER FLJ20712 RP9 RP9P NPSR1-AS1 DPY19L1 MIR550B2 MIR548N BBS9 DPY19L1P2 ZNRF2P1 NPSR1
esv2734229	Chr.7:32916268 - 33093711 on Build GRCh38	Deletion	NT5C3A RP9P FKBP9
nsv1135982	Chr.7:32794601 - 34893593 on Build GRCh38	Deletion	NT5C3A KBTBD2 RP9P NPSR1-AS1 LOC100421336 FKBP9 BBS9 DPY19L1P2 NPSR1 BMPER FLJ20712 RP9
nsv436907	Chr.7:32668474 - 34999437 on Build GRCh38	Insertion	DPY19L1P1 MIR550A2 NT5C3A KBTBD2 LOC100421336 FKBP9 LINC00997 BMPER FLJ20712 RP9 RP9P NPSR1-AS1 DPY19L1 MIR550B2 MIR548N BBS9 DPY19L1P2 ZNRF2P1 NPSR1

More Information

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