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

Chr.1:2215192 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03359715_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:

 Overlaps - Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC105378592 XM_017003075.1 XP_016858564.1
XM_017003076.1 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 C1orf159 UBE2J2 WASH7P LOC105378591 LOC100134822 DDX11L1 LINC01342 TTLL10 MIR1302-2 LOC102725121 VWA1 MIR6859-1 FNDC10 LOC100288175 ATAD3B OR4F16 LOC102724312 TAS1R3 LOC100132287 PLEKHN1 TTLL10-AS1 MTND2P28 PUSL1 LOC105378948 LOC100133331 LOC100129534 MTND1P23 MMP23B CALML6 ISG15 CFAP74 PRKCZ SLC35E2 SLC35E2B CPSF3L AGRN MIB2 LOC729737 ATAD3A MMP23A FAM41C PERM1 CCNL2 SCNN1D TMEM240 LOC107985729 GNB1 MIR6727 SDF4 MIR6859-2 TNFRSF4 KLHL17 FAM132A LOC100130417 DVL1 B3GALT6 RNF223 LOC105378947 AURKAIP1 CPTP CDK11B HES4 NOC2L FAM138A OR4F29 MORN1 MIR6726 MXRA8 LOC107984841 SKI TMEM52 LOC100288069 MRPL20 LOC100287934 LOC101928626 LOC148413 TMEM88B LINC00115 SAMD11 MIR200A NADK FAAP20 OR4F5 LOC284600 TNFRSF18 CDK11A ACAP3 FAM87B LINC01128 GABRD LOC105378949 LOC105378592 MIR429 MIR200B LOC100506504 LOC107985728 LOC105378589 ANKRD65 SSU72 ATAD3C MIR6808 MIR6723
dgv49n54 Chr.1:2151050 - 2289783 on Build GRCh38 Loss SKI PRKCZ LOC100506504 FAAP20 LOC105378592
nsv951530 Chr.1:2153662 - 2229961 on Build GRCh38 Deletion SKI PRKCZ LOC100506504 FAAP20 LOC105378592
nsv470682 Chr.1:2188394 - 2378754 on Build GRCh38 Loss SKI MORN1 FAAP20 LOC100129534 LOC105378592
nsv834557 Chr.1:2117631 - 2311104 on Build GRCh38 Loss SKI PRKCZ LOC100506504 FAAP20 LOC105378592
nsv818111 Chr.1:2208822 - 2224923 on Build GRCh38 Loss FAAP20 LOC105378592

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

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