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

Chr.1:2214103 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03334974_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 1091 XP_016858564.1
XM_017003076.1 1 1091 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 ANKRD65 MIR6723 OR4F5 SLC35E2 FAM138A CDK11A CFAP74 LOC100133331 LOC107985729 MIR1302-2 GABRD MIR6727 LINC01342 CCNL2 MORN1 RNF223 MIB2 GNB1 LOC148413 FAAP20 LOC100132287 VWA1 SLC35E2B HES4 DDX11L1 LOC102724312 SDF4 MIR200B LOC100130417 LOC105378947 LINC01128 LINC00115 OR4F16 ACAP3 TMEM52 PUSL1 AURKAIP1 CDK11B DVL1 MTND1P23 PERM1 SCNN1D ATAD3B MXRA8 ISG15 MTND2P28 ATAD3C LOC102725121 TMEM88B LOC107985728 LOC105378589 CALML6 LOC105378592 NOC2L TMEM240 MIR6859-2 LOC100288069 LOC100506504 FAM87B LOC729737 WASH7P LOC105378591 MIR6726 PLEKHN1 LOC105378948 LOC100288175 MRPL20 LOC100134822 SAMD11 MIR6859-1 SSU72 ATAD3A MIR429 LOC101928626 MMP23B MIR200A KLHL17 OR4F29 PRKCZ TTLL10-AS1 TNFRSF4 LOC284600 CPTP UBE2J2 LOC105378949 TTLL10 FAM132A MMP23A LOC107984841 TAS1R3 LOC100129534 SKI CPSF3L NADK FAM41C AGRN FNDC10 LOC100287934 MIR6808 TNFRSF18 B3GALT6 C1orf159
dgv49n54 Chr.1:2151050 - 2289783 on Build GRCh38 Loss LOC100506504 FAAP20 PRKCZ SKI LOC105378592
nsv951530 Chr.1:2153662 - 2229961 on Build GRCh38 Deletion LOC100506504 FAAP20 PRKCZ SKI LOC105378592
nsv470682 Chr.1:2188394 - 2378754 on Build GRCh38 Loss FAAP20 LOC100129534 SKI MORN1 LOC105378592
nsv834557 Chr.1:2117631 - 2311104 on Build GRCh38 Loss LOC100506504 FAAP20 PRKCZ SKI 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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