Hs04364889_cn

• Gene Symbol: EGFL7
• Assay Reference Genome Location: Chr.9:136656424 on build GRCh38
• Cytoband: 9q34.3

Target Gene Details

• Entrez Gene ID: 51162
• Gene Name: EGF like domain multiple 7
• Gene Aliases: NEU1, VE-STATIN, ZNEU1
• Location: Chr.9:136654753-136672678 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
EGFL7

Target Gene Details

• Entrez Gene ID: 101928612
• Gene Name: uncharacterized LOC101928612
• Gene Aliases: -
• Location: Chr.9:136648610-136660421 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HSPC324	NR_135132.1
	AF161442.1			AAF29002.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv13005n54	Chr.9:136605258 - 136696482 on Build GRCh38	Loss	EGFL7 MIR126 LINC01451 HSPC324 AGPAT2
nsv509334	Chr.9:136514168 - 136724663 on Build GRCh38	Insertion	EGFL7 SNHG7 MIR4673 MIR126 LINC01451 FAM69B MIR4674 NOTCH1 HSPC324 AGPAT2 NALT1
nsv951203	Chr.9:136562849 - 136770848 on Build GRCh38	Deletion	LCN15 MIR6722 LINC01451 FAM69B LCN8 SNORA17B HSPC324 EGFL7 LOC100128593 SNHG7 MIR126 SNORA17A LCN10 AGPAT2 LCN6
esv2759720	Chr.9:136356377 - 136932033 on Build GRCh38	Loss	LCN15 DNLZ FAM69B LCN8 MIR4479 PMPCA NOTCH1 SNORA17B HSPC324 PHPT1 TRAF2 EGFL7 C9orf172 LOC100128593 SNHG7 EDF1 CCDC183 MAMDC4 SNORA17A TMEM141 LCN6 CCDC183-AS1 MIR4673 CARD9 SNAPC4 MIR4292 MIR6722 LINC01451 RABL6 SDCCAG3 C9orf163 MIR126 SEC16A MIR4674 GPSM1 LCN10 AGPAT2 INPP5E NALT1
nsv469918	Chr.9:136359865 - 137173890 on Build GRCh38	Loss	LCN15 CLIC3 MIR4479 PMPCA PHPT1 DPP7 C9orf172 LOC100128593 SNHG7 C9orf139 CCDC183 MAMDC4 SAPCD2 PRR31 SNORA17A CCDC183-AS1 CARD9 ENTPD2 PTGDS RABL6 UAP1L1 C8G C9orf163 MAN1B1-AS1 GRIN1 SEC16A MIR4674 LCN10 AGPAT2 NPDC1 NALT1 DNLZ MIR3621 FAM69B LCN8 LCNL1 NOTCH1 SNORA17B HSPC324 FUT7 TRAF2 C9orf142 EGFL7 LCN12 FBXW5 EDF1 LRRC26 TMEM141 LCN6 MIR4673 ABCA2 SNAPC4 MIR4292 MIR6722 LINC01451 TMEM210 SDCCAG3 MIR126 MAN1B1 LOC101930307 INPP5E
nsv8579	Chr.9:136505432 - 136760256 on Build GRCh38	Gain	LCN15 MIR4673 MIR6722 LINC01451 FAM69B LCN8 NOTCH1 SNORA17B HSPC324 EGFL7 LOC100128593 SNHG7 MIR126 MIR4674 SNORA17A LCN10 AGPAT2 LCN6 NALT1
dgv955n27	Chr.9:136583078 - 136676165 on Build GRCh38	Loss	EGFL7 MIR126 LINC01451 HSPC324 AGPAT2
nsv1053781	Chr.9:136590694 - 136722927 on Build GRCh38	Gain	EGFL7 MIR126 LINC01451 FAM69B HSPC324 AGPAT2
dgv13006n54	Chr.9:136619086 - 136725859 on Build GRCh38	Loss	EGFL7 SNHG7 MIR126 FAM69B HSPC324 AGPAT2
esv2422220	Chr.9:136584135 - 137350098 on Build GRCh38	Deletion	LCN15 EXD3 CLIC3 MIR4479 PHPT1 DPP7 C9orf172 LOC100128593 SNHG7 TMEM203 C9orf139 CCDC183 MAMDC4 SAPCD2 PRR31 SNORA17A SLC34A3 NELFB TOR4A CCDC183-AS1 ENTPD2 PTGDS RABL6 UAP1L1 RNF224 C8G FAM166A MAN1B1-AS1 STPG3 RNF208 GRIN1 LCN10 AGPAT2 NPDC1 C9orf173-AS1 MIR3621 FAM69B LCN8 LCNL1 SNORA17B HSPC324 FUT7 TRAF2 C9orf142 EGFL7 NDOR1 LCN12 FBXW5 EDF1 LRRC26 TMEM141 LCN6 SSNA1 ABCA2 MIR4292 MIR6722 LINC01451 TUBB4B TMEM210 CYSRT1 TPRN NRARP MIR126 ANAPC2 MAN1B1 LOC101930307

More Information

Additional Information:

For this assay, SNP(s) [rs79218093] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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