Genomic Map
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Target Gene Details
Entrez Gene ID: | 125704 |
Gene Name: | family with sequence similarity 69 member C |
Gene Aliases: |
C18orf51 |
Location: |
Chr.18:74432575-74464646 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM69C | XM_017025551.1 | XP_016881040.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3643119 | Chr.18:74457578 - 74467353 on Build GRCh38 | Gain |
 FAM69C
|
| nsv577653 | Chr.18:74436411 - 74471994 on Build GRCh38 | Gain |
FAM69C
|
| nsv1057441 | Chr.18:74344906 - 74669985 on Build GRCh38 | Gain |
CNDP1
ZNF407
LOC101927606
FAM69C
LINC00909
CNDP2
C18orf63
|
| esv3643117 | Chr.18:74454714 - 74614537 on Build GRCh38 | Loss |
CNDP1
ZNF407
FAM69C
LINC00909
CNDP2
|
| nsv577654 | Chr.18:74445966 - 74467617 on Build GRCh38 | Gain |
FAM69C
|
| nsv527671 | Chr.18:74415709 - 74476151 on Build GRCh38 | Gain |
FAM69C
|
| esv1000434 | Chr.18:74422735 - 74465401 on Build GRCh38 | Deletion |
FAM69C
|
| nsv577655 | Chr.18:74463196 - 74504009 on Build GRCh38 | Loss |
FAM69C
CNDP2
|
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Intragenic