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See other LOC102723722 CNV Assays ›
Gene Symbol
LOC102723722
Assay Reference Genome
Location

Chr.22:42132810 on build GRCh38
Cytoband
22q13.2
Assay ID Hs04504210_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 102723722

Gene Name:

 uncharacterized LOC102723722

Gene Aliases:

 -

Location:

 Chr.22:42128862-42137554 on Build GRCh38

Assay Gene Location:
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC102723722

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1139782 Chr.22:42129998 - 42145299 on Build GRCh38 Duplication CYP2D7 CYP2D6 LOC102723722
dgv1319e212 Chr.22:42126516 - 42145482 on Build GRCh38 Gain CYP2D7 CYP2D6 LOC102723722
esv6632 Chr.22:42125966 - 42139888 on Build GRCh38 Loss CYP2D6 LOC102723722
esv3568417 Chr.22:42126951 - 42144107 on Build GRCh38 Loss CYP2D7 CYP2D6 LOC102723722
nsv498989 Chr.22:42123210 - 42135371 on Build GRCh38 Loss CYP2D6 NDUFA6-AS1 LOC102723722
esv2171396 Chr.22:42125911 - 42139869 on Build GRCh38 Deletion CYP2D6 LOC102723722
esv3349998 Chr.22:42132201 - 42137597 on Build GRCh38 Duplication LOC102723722
nsv1076539 Chr.22:42130197 - 42144099 on Build GRCh38 Duplication CYP2D7 CYP2D6 LOC102723722
nsv834210 Chr.22:42057329 - 42209100 on Build GRCh38 Loss TCF20 SNORD13P1 NDUFA6 NAGA WBP2NL CYP2D7 CYP2D6 NDUFA6-AS1 LOC102723722 SMDT1 FAM109B
esv3446082 Chr.22:42129806 - 42136897 on Build GRCh38 Duplication CYP2D6 LOC102723722
esv3575484 Chr.22:42118886 - 42144107 on Build GRCh38 Gain CYP2D7 CYP2D6 NDUFA6-AS1 LOC102723722
esv27312 Chr.22:42121254 - 42154514 on Build GRCh38 Gain+Loss CYP2D7 CYP2D6 NDUFA6-AS1 LOC102723722
nsv508737 Chr.22:42052007 - 42134336 on Build GRCh38 Insertion SNORD13P1 NDUFA6 NAGA WBP2NL CYP2D6 NDUFA6-AS1 LOC102723722 SMDT1 FAM109B
nsv1110402 Chr.22:42125795 - 42137591 on Build GRCh38 Duplication CYP2D6 LOC102723722
esv33893 Chr.22:42126620 - 42142218 on Build GRCh38 Gain+Loss CYP2D7 CYP2D6 LOC102723722
esv3647809 Chr.22:42127947 - 42137882 on Build GRCh38 Loss CYP2D6 LOC102723722
dgv733e201 Chr.22:42128848 - 42143382 on Build GRCh38 Deletion CYP2D7 CYP2D6 LOC102723722
nsv436350 Chr.22:42125831 - 42135447 on Build GRCh38 Deletion CYP2D6 LOC102723722
esv2724275 Chr.22:42123193 - 42141302 on Build GRCh38 Deletion CYP2D7 CYP2D6 NDUFA6-AS1 LOC102723722
nsv3641 Chr.22:42099466 - 42146296 on Build GRCh38 Deletion CYP2D7 CYP2D6 NDUFA6-AS1 LOC102723722
nsv955164 Chr.22:42122897 - 42144299 on Build GRCh38 Deletion CYP2D7 CYP2D6 NDUFA6-AS1 LOC102723722

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More Information


Important Information

Individuals may carry null alleles or extra copies of CYP2D6. Some CYP2D6 alleles contain sequences derived from the highly homologous CYP2D7 pseudogene. Hs04504210_cn specifically targets CYP2D6 5' upstream region sequences and will not amplify CYP2D7 or CYP2D8 pseudogenes, but will amplify CYP2D6/CYP2D7 hybrid alleles carrying CYP2D6 5' upstream sequences (e.g. CYP2D6*36, *68, etc.).

Additional Information:

Set Membership:

 Intragenic Non-exonic DGV Variation Validated

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