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See other FLJ37453 CNV Assays ›
Gene Symbol
FLJ37453
Assay Reference Genome
Location

Chr.1:15834399 on build GRCh38
Cytoband
1p36.21
Assay ID Hs03368575_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

729614

Gene Name:

uncharacterized LOC729614

Gene Aliases:

-

Location:

Chr.1:15834215-15848147 on Build GRCh38

Assay Gene Location:

Within Exon 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FLJ37453 NR_024279.1 2 2548
AK094772.1 1 1462 BAC04420.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv524044 Chr.1:15675093 - 15835341 on Build GRCh38 Loss FLJ37453 FBLIM1 UQCRHL SLC25A34 PLEKHM2 TMEM82
nsv1011969 Chr.1:15826990 - 15875045 on Build GRCh38 Gain+Loss FLJ37453 SPEN
dgv154n54 Chr.1:15827003 - 15834894 on Build GRCh38 Loss FLJ37453
nsv833647 Chr.1:15794042 - 15952334 on Build GRCh38 Loss FLJ37453 SPEN UQCRHL ZBTB17
nsv545619 Chr.1:15802946 - 15834894 on Build GRCh38 Loss FLJ37453 UQCRHL
nsv511126 Chr.1:15822806 - 15835341 on Build GRCh38 Loss FLJ37453
dgv37n100 Chr.1:15823408 - 15924038 on Build GRCh38 Gain FLJ37453 SPEN
esv2764241 Chr.1:15827002 - 15855150 on Build GRCh38 Loss FLJ37453 SPEN
nsv3409 Chr.1:15809988 - 15852694 on Build GRCh38 Deletion FLJ37453 SPEN

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More Information


Set Membership:

Intragenic Exonic DGV Variation

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