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

Chr.1:2213617 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03359165_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 1577 XP_016858564.1
XM_017003076.1 1 1577 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 SDF4 PRKCZ SSU72 LOC107984841 CDK11A TNFRSF4 NOC2L PUSL1 LOC100133331 TMEM88B OR4F16 LOC107985729 LOC100132287 SKI FAM138A MIB2 FAM41C LOC100288175 MMP23B MMP23A TMEM240 HES4 FNDC10 LOC105378948 LOC148413 MIR429 ACAP3 MORN1 MIR200A AURKAIP1 FAM87B MIR6859-2 LINC01342 LOC100288069 LOC729737 CPSF3L ATAD3C LOC100129534 FAM132A TTLL10-AS1 LINC01128 OR4F29 SLC35E2B MIR200B LOC100287934 TTLL10 KLHL17 MIR6808 ANKRD65 MIR6723 LOC100506504 DDX11L1 RNF223 LOC100134822 PERM1 GNB1 NADK LOC105378947 SAMD11 CALML6 MIR6727 MIR6859-1 C1orf159 TMEM52 LOC107985728 CDK11B LOC100130417 LOC105378591 ATAD3A LOC102725121 LOC284600 UBE2J2 CFAP74 MTND2P28 MIR6726 PLEKHN1 LOC102724312 TAS1R3 OR4F5 LOC105378949 B3GALT6 MIR1302-2 LOC105378592 CPTP WASH7P MTND1P23 SLC35E2 DVL1 LINC00115 GABRD CCNL2 ISG15 AGRN TNFRSF18 VWA1 ATAD3B LOC105378589 MXRA8 LOC101928626 FAAP20 SCNN1D MRPL20
dgv49n54 Chr.1:2151050 - 2289783 on Build GRCh38 Loss SKI LOC105378592 PRKCZ FAAP20 LOC100506504
nsv951530 Chr.1:2153662 - 2229961 on Build GRCh38 Deletion SKI LOC105378592 PRKCZ FAAP20 LOC100506504
nsv470682 Chr.1:2188394 - 2378754 on Build GRCh38 Loss LOC100129534 SKI LOC105378592 FAAP20 MORN1
nsv834557 Chr.1:2117631 - 2311104 on Build GRCh38 Loss SKI LOC105378592 PRKCZ FAAP20 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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