Hs03702994_cn

• Gene Symbol: EGFL7
• Assay Reference Genome Location: Chr.9:136657237 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	HSPC324 LINC01451 EGFL7 MIR126 AGPAT2
esv2739380	Chr.9:136656625 - 136657890 on Build GRCh38	Deletion	HSPC324 EGFL7
nsv509334	Chr.9:136514168 - 136724663 on Build GRCh38	Insertion	MIR4674 HSPC324 NALT1 SNHG7 LINC01451 EGFL7 NOTCH1 MIR126 MIR4673 AGPAT2 FAM69B
nsv951203	Chr.9:136562849 - 136770848 on Build GRCh38	Deletion	HSPC324 SNHG7 LINC01451 MIR6722 EGFL7 MIR126 AGPAT2 LCN15 SNORA17A LCN8 SNORA17B LCN6 LOC100128593 LCN10 FAM69B
esv2759720	Chr.9:136356377 - 136932033 on Build GRCh38	Loss	CARD9 C9orf172 DNLZ NALT1 RABL6 MIR126 CCDC183 AGPAT2 PHPT1 EDF1 TMEM141 GPSM1 MAMDC4 PMPCA MIR4292 NOTCH1 MIR4674 INPP5E C9orf163 HSPC324 SNAPC4 SNHG7 LINC01451 MIR6722 CCDC183-AS1 EGFL7 SEC16A SDCCAG3 LCN15 SNORA17A LCN8 TRAF2 SNORA17B LCN6 LOC100128593 MIR4479 LCN10 MIR4673 FAM69B
nsv469918	Chr.9:136359865 - 137173890 on Build GRCh38	Loss	C9orf139 RABL6 MIR126 AGPAT2 PHPT1 EDF1 TMEM141 MAMDC4 PMPCA MIR4292 C9orf142 MAN1B1 NOTCH1 UAP1L1 INPP5E C9orf163 LCNL1 HSPC324 SNHG7 MIR6722 CCDC183-AS1 SEC16A C8G SDCCAG3 LCN8 PRR31 ABCA2 LOC100128593 FUT7 MIR4673 CARD9 CLIC3 C9orf172 DNLZ NALT1 PTGDS LCN12 LOC101930307 GRIN1 CCDC183 ENTPD2 DPP7 MIR4674 SNAPC4 NPDC1 MAN1B1-AS1 LINC01451 EGFL7 TMEM210 LCN15 SNORA17A SAPCD2 MIR3621 TRAF2 FBXW5 SNORA17B LCN6 MIR4479 LCN10 LRRC26 FAM69B
nsv8579	Chr.9:136505432 - 136760256 on Build GRCh38	Gain	MIR4674 HSPC324 NALT1 SNHG7 LINC01451 MIR6722 EGFL7 MIR126 AGPAT2 LCN15 SNORA17A LCN8 SNORA17B LCN6 LOC100128593 NOTCH1 LCN10 MIR4673 FAM69B
esv8966	Chr.9:136656498 - 136657933 on Build GRCh38	Loss	HSPC324 EGFL7
dgv955n27	Chr.9:136583078 - 136676165 on Build GRCh38	Loss	HSPC324 LINC01451 EGFL7 MIR126 AGPAT2
nsv1053781	Chr.9:136590694 - 136722927 on Build GRCh38	Gain	HSPC324 LINC01451 EGFL7 MIR126 AGPAT2 FAM69B
dgv13006n54	Chr.9:136619086 - 136725859 on Build GRCh38	Loss	HSPC324 SNHG7 EGFL7 MIR126 AGPAT2 FAM69B
esv2422220	Chr.9:136584135 - 137350098 on Build GRCh38	Deletion	CYSRT1 C9orf139 RABL6 SLC34A3 MIR126 AGPAT2 PHPT1 EDF1 TMEM141 MAMDC4 MIR4292 C9orf142 MAN1B1 UAP1L1 LCNL1 HSPC324 EXD3 SNHG7 MIR6722 CCDC183-AS1 C8G LCN8 SSNA1 PRR31 ABCA2 LOC100128593 FUT7 CLIC3 C9orf172 NRARP PTGDS LCN12 STPG3 LOC101930307 GRIN1 CCDC183 TOR4A FAM166A C9orf173-AS1 ENTPD2 DPP7 RNF224 NPDC1 TMEM203 MAN1B1-AS1 LINC01451 NELFB EGFL7 TMEM210 TUBB4B ANAPC2 RNF208 LCN15 SNORA17A SAPCD2 MIR3621 NDOR1 TRAF2 FBXW5 SNORA17B LCN6 MIR4479 LCN10 TPRN LRRC26 FAM69B

More Information

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