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

More Information

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