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

Chr.1:2213303 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03379191_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 1891 XP_016858564.1
XM_017003076.1 1 1891 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 TTLL10-AS1 FNDC10 PRKCZ LOC105378947 TTLL10 PLEKHN1 ISG15 NOC2L CPTP OR4F16 AURKAIP1 LOC107985728 FAAP20 DDX11L1 VWA1 LOC100132287 OR4F5 WASH7P OR4F29 MIR6859-1 LOC105378589 LOC100288175 LOC102724312 FAM132A MMP23A MIR6808 TAS1R3 CALML6 LOC105378948 TMEM88B SLC35E2 PUSL1 DVL1 LOC105378591 ACAP3 MIR429 MRPL20 MIR200A ATAD3B LINC01342 HES4 MIB2 CCNL2 ATAD3A TMEM52 CPSF3L GNB1 LOC100288069 MIR6726 SAMD11 LOC100506504 LOC100287934 RNF223 FAM138A SLC35E2B FAM87B MTND2P28 SKI MIR1302-2 NADK TNFRSF18 FAM41C MORN1 SCNN1D LOC105378949 LOC100130417 UBE2J2 LOC148413 LINC00115 MTND1P23 CDK11B GABRD LOC284600 PERM1 MIR6859-2 C1orf159 B3GALT6 MIR6727 MMP23B TMEM240 LOC107985729 LOC729737 LOC100129534 MIR6723 SDF4 LOC100133331 MXRA8 CDK11A TNFRSF4 SSU72 LOC107984841 LOC102725121 LOC101928626 AGRN ATAD3C MIR200B CFAP74 LINC01128 ANKRD65 KLHL17 LOC100134822 LOC105378592
dgv49n54 Chr.1:2151050 - 2289783 on Build GRCh38 Loss SKI PRKCZ FAAP20 LOC100506504 LOC105378592
nsv951530 Chr.1:2153662 - 2229961 on Build GRCh38 Deletion SKI PRKCZ FAAP20 LOC100506504 LOC105378592
nsv470682 Chr.1:2188394 - 2378754 on Build GRCh38 Loss SKI LOC100129534 MORN1 FAAP20 LOC105378592
nsv834557 Chr.1:2117631 - 2311104 on Build GRCh38 Loss SKI PRKCZ FAAP20 LOC100506504 LOC105378592
nsv818111 Chr.1:2208822 - 2224923 on Build GRCh38 Loss FAAP20 LOC105378592

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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