Hs01555996_cn

• Gene Symbol: CCDC183
• Assay Reference Genome Location: Chr.9:136806620 on build GRCh38
• Cytoband: 9q34.3

Target Gene Details

• Entrez Gene ID: 84960
• Gene Name: coiled-coil domain containing 183
• Gene Aliases: KIAA1984, PARF, bA216L13.7
• Location: Chr.9:136796338-136807741 on Build GRCh38
• Assay Gene Location: Within Exon 11

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC183	NM_001039374.4	11	1286	NP_001034463.4
	AK090683.1	6	1127	BAC03504.1
	AK092639.1	7	1809	BAC03931.1
	AK094220.1	1	972
	BC064582.1	11	1272	AAH64582.1
	BC137317.1	11	1261
	BC137318.1	11	1261

Target Gene Details

• Entrez Gene ID: 100131193
• Gene Name: CCDC183 antisense RNA 1
• Gene Aliases: KIAA1984-AS1
• Location: Chr.9:136803927-136808848 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC183-AS1	NR_024580.1
	AK055547.1			BAB70952.1
	DA710348.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
dgv1246n67	Chr.9:136806360 - 136823613 on Build GRCh38	Gain	CCDC183 CCDC183-AS1 RABL6
nsv818738	Chr.9:136740043 - 137009585 on Build GRCh38	Gain	C9orf172 LCN8 MIR4292 LCN10 C8G LCN15 PRR31 MAMDC4 EDF1 MIR4479 PHPT1 PTGDS LCN6 RABL6 TRAF2 LOC100128593 CLIC3 LCNL1 TMEM141 CCDC183-AS1 MIR6722 CCDC183 ABCA2 C9orf142 LCN12 FBXW5
nsv951204	Chr.9:136803249 - 136807748 on Build GRCh38	Deletion	CCDC183 CCDC183-AS1
esv29973	Chr.9:136795692 - 136859658 on Build GRCh38	Loss	C9orf172 CCDC183 MIR4292 MAMDC4 CCDC183-AS1 PHPT1 RABL6
nsv469918	Chr.9:136359865 - 137173890 on Build GRCh38	Loss	UAP1L1 LRRC26 MIR4292 C8G FAM69B LCN15 PMPCA PRR31 MIR4674 MAN1B1 NALT1 MAMDC4 C9orf139 EDF1 DNLZ PHPT1 LOC101930307 PTGDS MAN1B1-AS1 LOC100128593 INPP5E CLIC3 HSPC324 LCNL1 TMEM141 CCDC183-AS1 MIR6722 NOTCH1 SDCCAG3 ABCA2 C9orf142 C9orf163 GRIN1 SNAPC4 MIR3621 LCN12 C9orf172 LINC01451 LCN8 SNORA17A AGPAT2 LCN10 FUT7 SNHG7 SEC16A MIR4479 LCN6 SAPCD2 MIR126 RABL6 TRAF2 NPDC1 TMEM210 CARD9 ENTPD2 SNORA17B EGFL7 CCDC183 DPP7 MIR4673 FBXW5
esv2759720	Chr.9:136356377 - 136932033 on Build GRCh38	Loss	C9orf172 LINC01451 LCN8 MIR4292 SNORA17A AGPAT2 LCN10 FAM69B LCN15 PMPCA MIR4674 NALT1 MAMDC4 SNHG7 SEC16A EDF1 MIR4479 DNLZ PHPT1 LCN6 MIR126 RABL6 TRAF2 LOC100128593 INPP5E HSPC324 GPSM1 CARD9 TMEM141 CCDC183-AS1 MIR6722 SNORA17B EGFL7 NOTCH1 CCDC183 SDCCAG3 C9orf163 MIR4673 SNAPC4
esv2422220	Chr.9:136584135 - 137350098 on Build GRCh38	Deletion	UAP1L1 NELFB C9orf173-AS1 STPG3 LRRC26 SLC34A3 MIR4292 C8G FAM69B TOR4A LCN15 PRR31 MAN1B1 MAMDC4 C9orf139 EDF1 TMEM203 PHPT1 LOC101930307 PTGDS CYSRT1 MAN1B1-AS1 LOC100128593 CLIC3 HSPC324 LCNL1 TMEM141 SSNA1 CCDC183-AS1 FAM166A MIR6722 ANAPC2 TUBB4B ABCA2 C9orf142 GRIN1 MIR3621 LCN12 C9orf172 LINC01451 LCN8 SNORA17A AGPAT2 NRARP LCN10 EXD3 FUT7 RNF208 SNHG7 MIR4479 LCN6 SAPCD2 MIR126 RABL6 TPRN NDOR1 TRAF2 NPDC1 TMEM210 ENTPD2 SNORA17B EGFL7 RNF224 CCDC183 DPP7 FBXW5

More Information

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