Hs03711792_cn

• Gene Symbol: HSPC324
• Assay Reference Genome Location: Chr.9:136649034 on build GRCh38
• Cytoband: 9q34.3

Target Gene Details

• Entrez Gene ID: 101928612
• Gene Name: uncharacterized LOC101928612
• Gene Aliases: -
• Location: Chr.9:136648610-136660421 on Build GRCh38
• Assay Gene Location: Overlaps Intron 1 - Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HSPC324	NR_135132.1
	AF161442.1			AAF29002.1
	BE466352.1

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

More Information

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