Hs01234949_cn

• Gene Symbol: CCDC183
• Assay Reference Genome Location: Chr.9:136807633 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 Intron 13 - Exon 14

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	1883
	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 Intron 1

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

More Information

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