Hs01877487_cn

• Gene Symbol: CCDC183
• Assay Reference Genome Location: Chr.9:136807053 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: Overlaps Exon 13 - Intron 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC183	NM_001039374.4			NP_001034463.4
	AK090683.1			BAC03504.1
	AK092639.1			BAC03931.1
	AK094220.1	2	1303
	AW572474.1
	BC064582.1			AAH64582.1
	BC137317.1
	BC137318.1

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 Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC183-AS1	NR_024580.1	2	272
	AK055547.1	2	272	BAB70952.1
	DA710348.1	2	210

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

More Information

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