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See other LOC105378592 CNV Assays ›
Gene Symbol
LOC105378592
Assay Reference Genome
Location

Chr.1:2214527 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03356301_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 105378592

Gene Name:

 uncharacterized LOC105378592

Gene Aliases:

 -

Location:

 Chr.1:2207597-2215193 on Build GRCh38

Assay Gene Location:

 Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC105378592 XM_017003075.1 1 667 XP_016858564.1
XM_017003076.1 1 667 XP_016858565.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss PERM1 TNFRSF18 LINC01128 B3GALT6 FAM87B AGRN MXRA8 CPTP SAMD11 TNFRSF4 DVL1 MMP23B FAM132A TTLL10-AS1 LOC107985729 MIB2 SCNN1D LOC284600 MMP23A TMEM240 AURKAIP1 LOC729737 SKI SSU72 KLHL17 FAM138A ANKRD65 ATAD3A PUSL1 MTND1P23 MIR200B CFAP74 WASH7P CDK11A NOC2L ATAD3C LOC148413 LINC01342 LOC100287934 SDF4 MIR6726 C1orf159 LOC105378591 ISG15 MRPL20 MTND2P28 CPSF3L ATAD3B LOC100130417 LOC105378947 MIR200A DDX11L1 MIR6723 HES4 SLC35E2B LOC100133331 MIR6727 LOC100134822 LOC102724312 LOC105378948 LOC102725121 LOC101928626 LOC100132287 SLC35E2 ACAP3 FNDC10 MORN1 LOC107985728 NADK MIR6859-2 RNF223 LOC105378949 CDK11B OR4F16 LOC100288175 MIR6859-1 TMEM88B FAM41C TAS1R3 UBE2J2 TMEM52 CALML6 PRKCZ LOC100288069 PLEKHN1 MIR429 LOC105378589 MIR6808 TTLL10 MIR1302-2 OR4F29 LOC100506504 LOC105378592 FAAP20 GNB1 LOC100129534 GABRD OR4F5 CCNL2 VWA1 LINC00115 LOC107984841
dgv49n54 Chr.1:2151050 - 2289783 on Build GRCh38 Loss LOC105378592 SKI FAAP20 PRKCZ LOC100506504
nsv951530 Chr.1:2153662 - 2229961 on Build GRCh38 Deletion LOC105378592 SKI FAAP20 PRKCZ LOC100506504
nsv470682 Chr.1:2188394 - 2378754 on Build GRCh38 Loss LOC105378592 SKI FAAP20 MORN1 LOC100129534
nsv834557 Chr.1:2117631 - 2311104 on Build GRCh38 Loss LOC105378592 SKI FAAP20 PRKCZ LOC100506504
nsv818111 Chr.1:2208822 - 2224923 on Build GRCh38 Loss LOC105378592 FAAP20

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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