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

Chr.1:2214957 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03338805_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 1 237 XP_016858564.1
XM_017003076.1 1 237 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 GABRD SDF4 ACAP3 MIR6859-2 LOC100134822 TMEM88B LOC105378949 LINC00115 LINC01342 LOC729737 MIR6726 SCNN1D MTND1P23 LOC100129534 TTLL10-AS1 CCNL2 HES4 OR4F16 TNFRSF18 PERM1 TMEM240 LOC107985728 LOC107984841 MIR429 MIR1302-2 ATAD3B OR4F29 LOC100506504 MXRA8 C1orf159 FAM138A LINC01128 PRKCZ SAMD11 TTLL10 VWA1 FAM41C LOC105378589 LOC284600 ANKRD65 LOC100130417 MIR6723 MIR6808 MMP23B NADK LOC100288175 LOC102725121 MIR200B RNF223 CDK11A NOC2L B3GALT6 LOC105378947 FNDC10 CFAP74 FAM132A FAM87B DDX11L1 CPTP PLEKHN1 ATAD3C MTND2P28 MIR6859-1 AGRN GNB1 TMEM52 SLC35E2 MMP23A LOC148413 WASH7P LOC102724312 CPSF3L MRPL20 DVL1 MIR6727 MIR200A SSU72 ATAD3A LOC105378591 LOC100288069 LOC101928626 SLC35E2B TAS1R3 TNFRSF4 MORN1 MIB2 FAAP20 LOC100287934 ISG15 SKI PUSL1 LOC100133331 LOC105378592 LOC100132287 OR4F5 UBE2J2 CDK11B AURKAIP1 LOC107985729 LOC105378948 KLHL17 CALML6
dgv49n54 Chr.1:2151050 - 2289783 on Build GRCh38 Loss PRKCZ SKI LOC105378592 FAAP20 LOC100506504
nsv951530 Chr.1:2153662 - 2229961 on Build GRCh38 Deletion PRKCZ SKI LOC105378592 FAAP20 LOC100506504
nsv470682 Chr.1:2188394 - 2378754 on Build GRCh38 Loss SKI LOC105378592 MORN1 FAAP20 LOC100129534
nsv834557 Chr.1:2117631 - 2311104 on Build GRCh38 Loss PRKCZ SKI LOC105378592 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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