Hs03701375_cn

• Gene Symbol: EGFL7
• Assay Reference Genome Location: Chr.9:136656216 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	MIR126 HSPC324 LINC01451 EGFL7 AGPAT2
nsv509334	Chr.9:136514168 - 136724663 on Build GRCh38	Insertion	FAM69B MIR126 MIR4673 SNHG7 NOTCH1 HSPC324 LINC01451 NALT1 EGFL7 AGPAT2 MIR4674
nsv951203	Chr.9:136562849 - 136770848 on Build GRCh38	Deletion	MIR126 LCN15 LCN10 LOC100128593 LCN6 LINC01451 SNORA17B MIR6722 SNORA17A AGPAT2 LCN8 FAM69B SNHG7 HSPC324 EGFL7
nsv469918	Chr.9:136359865 - 137173890 on Build GRCh38	Loss	LCN15 NOTCH1 GRIN1 SNORA17B ABCA2 RABL6 SDCCAG3 INPP5E MIR4674 MAN1B1-AS1 TMEM210 FAM69B SEC16A NALT1 CLIC3 UAP1L1 DNLZ MAMDC4 C9orf139 PHPT1 LINC01451 NPDC1 PRR31 FBXW5 C9orf172 SNHG7 MIR4479 MIR3621 TRAF2 LRRC26 LCNL1 SNAPC4 PMPCA MIR126 CCDC183-AS1 LOC100128593 LCN6 CARD9 MIR6722 ENTPD2 LCN12 DPP7 C9orf142 MIR4292 MIR4673 FUT7 C8G PTGDS TMEM141 LCN10 CCDC183 MAN1B1 SNORA17A AGPAT2 LCN8 EDF1 HSPC324 C9orf163 SAPCD2 LOC101930307 EGFL7
esv2759720	Chr.9:136356377 - 136932033 on Build GRCh38	Loss	SNAPC4 PMPCA MIR126 LCN15 NOTCH1 CCDC183-AS1 LOC100128593 LCN6 SNORA17B CARD9 RABL6 SDCCAG3 MIR6722 INPP5E MIR4674 FAM69B MIR4292 MIR4673 SEC16A NALT1 DNLZ MAMDC4 GPSM1 TMEM141 LCN10 CCDC183 PHPT1 LINC01451 SNORA17A AGPAT2 LCN8 EDF1 C9orf172 SNHG7 MIR4479 HSPC324 C9orf163 TRAF2 EGFL7
nsv8579	Chr.9:136505432 - 136760256 on Build GRCh38	Gain	MIR126 LCN15 LCN10 NOTCH1 LOC100128593 LCN6 LINC01451 SNORA17B MIR6722 SNORA17A AGPAT2 MIR4674 LCN8 FAM69B MIR4673 SNHG7 HSPC324 NALT1 EGFL7
nsv615971	Chr.9:136583078 - 136670216 on Build GRCh38	Loss	HSPC324 LINC01451 EGFL7
nsv1053781	Chr.9:136590694 - 136722927 on Build GRCh38	Gain	FAM69B MIR126 HSPC324 LINC01451 EGFL7 AGPAT2
dgv957n27	Chr.9:136619086 - 136725859 on Build GRCh38	Loss	FAM69B MIR126 SNHG7 HSPC324 EGFL7 AGPAT2
esv2422220	Chr.9:136584135 - 137350098 on Build GRCh38	Deletion	LCN15 GRIN1 SNORA17B ABCA2 RABL6 NELFB MAN1B1-AS1 TMEM210 TOR4A FAM69B RNF224 CLIC3 NDOR1 UAP1L1 EXD3 MAMDC4 C9orf139 SSNA1 PHPT1 LINC01451 NPDC1 PRR31 FBXW5 NRARP C9orf172 SNHG7 MIR4479 MIR3621 TRAF2 LRRC26 LCNL1 ANAPC2 MIR126 CCDC183-AS1 LOC100128593 LCN6 SLC34A3 MIR6722 ENTPD2 LCN12 TMEM203 DPP7 C9orf142 FAM166A MIR4292 C9orf173-AS1 FUT7 C8G PTGDS TMEM141 LCN10 TPRN CCDC183 MAN1B1 SNORA17A AGPAT2 TUBB4B LCN8 EDF1 RNF208 STPG3 HSPC324 SAPCD2 CYSRT1 LOC101930307 EGFL7

More Information

Additional Information:

For this assay, SNP(s) [rs78750992] 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