Hs01528852_cn

• Gene Symbol: CCDC183
• Assay Reference Genome Location: Chr.9:136806779 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 11 - Exon 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC183	NM_001039374.4			NP_001034463.4
	AK090683.1			BAC03504.1
	AK092639.1	7	1968	BAC03931.1
	AK094220.1	1	1131
	AW572474.1
	BC064582.1	11	1431	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 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-AS1 CCDC183 RABL6
nsv818738	Chr.9:136740043 - 137009585 on Build GRCh38	Gain	ABCA2 MIR4292 CCDC183 PTGDS FBXW5 MIR4479 CCDC183-AS1 RABL6 LCN10 TRAF2 MIR6722 PRR31 CLIC3 C8G PHPT1 LCNL1 LCN6 C9orf172 MAMDC4 LCN12 LCN15 LCN8 LOC100128593 EDF1 C9orf142 TMEM141
nsv951204	Chr.9:136803249 - 136807748 on Build GRCh38	Deletion	CCDC183-AS1 CCDC183
esv29973	Chr.9:136795692 - 136859658 on Build GRCh38	Loss	C9orf172 MAMDC4 MIR4292 CCDC183-AS1 CCDC183 PHPT1 RABL6
nsv469918	Chr.9:136359865 - 137173890 on Build GRCh38	Loss	ABCA2 C9orf163 MIR4292 MIR3621 SNORA17B SDCCAG3 NALT1 MAN1B1-AS1 FBXW5 AGPAT2 SNHG7 INPP5E CCDC183-AS1 LOC101930307 LCN10 DPP7 CARD9 TRAF2 SNAPC4 GRIN1 UAP1L1 CLIC3 C8G PHPT1 LCN6 HSPC324 TMEM210 LCN8 MIR126 MAN1B1 EDF1 C9orf142 LRRC26 C9orf139 SNORA17A CCDC183 FUT7 SAPCD2 FAM69B PTGDS MIR4479 LINC01451 RABL6 MIR4673 MIR6722 EGFL7 PRR31 MIR4674 DNLZ NOTCH1 LCNL1 NPDC1 C9orf172 MAMDC4 LCN12 LCN15 PMPCA LOC100128593 SEC16A TMEM141 ENTPD2
esv2759720	Chr.9:136356377 - 136932033 on Build GRCh38	Loss	C9orf163 MIR4292 SNORA17A SNORA17B CCDC183 SDCCAG3 FAM69B NALT1 AGPAT2 SNHG7 INPP5E MIR4479 LINC01451 CCDC183-AS1 RABL6 MIR4673 LCN10 CARD9 TRAF2 SNAPC4 MIR6722 EGFL7 GPSM1 MIR4674 DNLZ PHPT1 NOTCH1 LCN6 HSPC324 C9orf172 MAMDC4 LCN15 PMPCA LCN8 MIR126 LOC100128593 EDF1 SEC16A TMEM141
esv2422220	Chr.9:136584135 - 137350098 on Build GRCh38	Deletion	ABCA2 MIR4292 C9orf173-AS1 MIR3621 SNORA17B MAN1B1-AS1 FBXW5 AGPAT2 SNHG7 CCDC183-AS1 LOC101930307 NDOR1 LCN10 DPP7 TRAF2 GRIN1 UAP1L1 RNF224 NELFB CLIC3 C8G PHPT1 NRARP LCN6 HSPC324 TMEM210 LCN8 MIR126 CYSRT1 TOR4A MAN1B1 EDF1 C9orf142 EXD3 LRRC26 C9orf139 SNORA17A ANAPC2 CCDC183 FUT7 SAPCD2 FAM166A FAM69B PTGDS MIR4479 LINC01451 TPRN RABL6 MIR6722 EGFL7 SSNA1 PRR31 STPG3 RNF208 TMEM203 LCNL1 NPDC1 C9orf172 MAMDC4 LCN12 LCN15 SLC34A3 LOC100128593 TUBB4B TMEM141 ENTPD2

More Information

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