Hs03712195_cn

• Gene Symbol: HSPC324
• Assay Reference Genome Location: Chr.9:136648728 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: Within Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HSPC324	NR_135132.1	2	439
	AF161442.1	2	440	AAF29002.1
	BE466352.1	1	118

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

More Information

• Set Membership: Intragenic, Exonic, DGV Variation