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See other OR2T10 CNV Assays ›
Gene Symbol
OR2T10
Assay Reference Genome
Location

Chr.1:248525263 on build GRCh38
Cytoband
1q44
Assay ID Hs04206355_cn
Size
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 127069

Gene Name:

 olfactory receptor family 2 subfamily T member 10

Gene Aliases:

 OR1-64

Location:

 Chr.1:248483404-248645469 on Build GRCh38

Assay Gene Location:
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
OR2T10

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2760083 Chr.1:248442451 - 248655182 on Build GRCh38 Gain+Loss OR2T29 OR2T35 OR2T27 OR2T5 OR2T10 OR2T11 OR2T3 OR2T34 OR2T2 OR2G6
nsv515858 Chr.1:247620588 - 248705477 on Build GRCh38 Gain+Loss OR2M7 TRIM58 OR2L8 OR2M5 OR2T8 OR2M3 OR14I1 LOC101928226 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 OR2T2 OR11L1 OR2T35 OR2T27 OR2L3 OR2AK2 OR2T33 OR2T3 OR2T34 OR14A16 OR2T1 OR2L1P OR2L13 OR6F1 OR2M4 OR9H1P OR2T5 OR2T10 OR2T12 OR1C1 OR2T11 OR2M2 OR13G1 OR2M1P OR2W3 OR2L5 OR14C36
dgv608n100 Chr.1:247907795 - 248631151 on Build GRCh38 Gain OR2M7 OR2L8 OR2M5 OR2T8 OR2M3 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 OR2T2 OR2L3 OR2AK2 OR2T33 OR2T3 OR2T34 OR2T1 OR2L1P OR2L13 OR2M4 OR2T5 OR2T10 OR2T12 OR2T11 OR2M2 OR2M1P OR2L5 OR14C36
nsv1009036 Chr.1:248442439 - 248534078 on Build GRCh38 Gain+Loss OR2T5 OR2T10 OR2T3 OR2T2 OR2G6
nsv428357 Chr.1:248336807 - 248714122 on Build GRCh38 Loss OR2T35 OR2T27 OR2T3 OR2T34 OR2T1 OR14I1 LOC101928226 OR2G6 OR2T29 OR2T4 OR2T5 OR2T10 OR2T11 OR2T6 OR14C36 OR2T2
dgv617n100 Chr.1:248457862 - 248605673 on Build GRCh38 Gain OR2T29 OR2T5 OR2T10 OR2T3 OR2T34 OR2G6
nsv821623 Chr.1:248481643 - 248627107 on Build GRCh38 Loss OR2T29 OR2T5 OR2T10 OR2T11 OR2T34 OR2G6
dgv606n100 Chr.1:247664654 - 248568732 on Build GRCh38 Gain OR2M7 TRIM58 OR2L8 OR2M5 OR2T8 OR2M3 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 OR2T2 OR11L1 OR2L3 OR2AK2 OR2T33 OR2T3 OR14A16 OR2T1 OR2L1P OR2L13 OR6F1 OR2M4 OR9H1P OR2T5 OR2T10 OR2T12 OR1C1 OR2M2 OR13G1 OR2M1P OR2W3 OR2L5 OR14C36
dgv906n54 Chr.1:248330209 - 248694378 on Build GRCh38 Gain OR2T35 OR2T27 OR2T3 OR2T34 OR2T1 OR14I1 OR2G6 OR2T29 OR2T4 OR2T5 OR2T10 OR2T11 OR2T6 OR14C36 OR2T2
nsv1013273 Chr.1:247656673 - 248784560 on Build GRCh38 Gain OR2M7 TRIM58 OR2L8 OR2M5 OR2T8 OR2M3 OR14I1 LOC101928226 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 LYPD8 OR2T2 OR11L1 OR2T35 OR2T27 OR2L3 OR2AK2 OR2T33 OR2T3 OR2T34 OR14A16 OR2T1 OR2L1P OR2L13 OR6F1 OR2M4 OR9H1P OR2T5 OR2T10 OR2T12 OR1C1 OR2T11 OR2M2 OR13G1 OR2M1P OR2W3 OR2L5 OR14C36
nsv549630 Chr.1:248214486 - 248525528 on Build GRCh38 Loss OR2M7 OR2T33 OR2T3 OR2T1 OR2G6 OR2T4 OR2M4 OR2T5 OR2T10 OR2T12 OR2T6 OR14C36 OR2T2
dgv17e55 Chr.1:248079226 - 248654081 on Build GRCh38 Loss OR2M7 OR2T35 OR2T27 OR2T33 OR2T3 OR2T34 OR2M5 OR2T1 OR2M3 OR2L13 OR2G6 OR2T29 OR2T4 OR2M4 OR2T5 OR2T10 OR2T12 OR2T11 OR2M2 OR2M1P OR2T6 OR14C36 OR2T2
dgv165e212 Chr.1:248520091 - 248670455 on Build GRCh38 Gain OR2T29 OR2T35 OR2T27 OR2T10 OR2T11 OR2T34 OR2G6
dgv607n100 Chr.1:247895273 - 248661824 on Build GRCh38 Loss OR2M7 OR2L8 OR2M5 OR2T8 OR2M3 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 OR2T2 OR2T35 OR2T27 OR2L3 OR2AK2 OR2T33 OR2T3 OR2T34 OR2T1 OR2L1P OR2L13 OR2M4 OR2T5 OR2T10 OR2T12 OR2T11 OR2M2 OR2M1P OR2W3 OR2L5 OR14C36
dgv619n100 Chr.1:248496871 - 248586247 on Build GRCh38 Gain OR2T29 OR2T10 OR2T34 OR2G6
dgv616n100 Chr.1:248436984 - 248574134 on Build GRCh38 Gain OR2T29 OR2T5 OR2T10 OR2T3 OR2T34 OR2T2 OR2G6
nsv549641 Chr.1:248450347 - 248622144 on Build GRCh38 Gain OR2T29 OR2T5 OR2T10 OR2T3 OR2T34 OR2T2 OR2G6
esv2763780 Chr.1:248520099 - 248650779 on Build GRCh38 Loss OR2T29 OR2T35 OR2T27 OR2T10 OR2T11 OR2T34 OR2G6
dgv620n100 Chr.1:248520087 - 248633900 on Build GRCh38 Loss OR2T29 OR2T10 OR2T11 OR2T34 OR2G6
dgv615n100 Chr.1:248432380 - 248550678 on Build GRCh38 Loss OR2T5 OR2T10 OR2T3 OR2T2 OR2G6
nsv1001494 Chr.1:248450022 - 248525287 on Build GRCh38 Gain OR2T5 OR2T10 OR2T3 OR2T2 OR2G6
esv3575950 Chr.1:248442438 - 248525271 on Build GRCh38 Gain OR2T5 OR2T10 OR2T3 OR2T2 OR2G6
dgv166e212 Chr.1:248524920 - 248664922 on Build GRCh38 Loss OR2T29 OR2T35 OR2T27 OR2T10 OR2T11 OR2T34
nsv1004790 Chr.1:248346193 - 248709345 on Build GRCh38 Gain OR2T35 OR2T27 OR2T3 OR2T34 OR2T1 OR14I1 LOC101928226 OR2G6 OR2T29 OR2T4 OR2T5 OR2T10 OR2T11 OR2T6 OR14C36 OR2T2
nsv549603 Chr.1:247885685 - 248672148 on Build GRCh38 Loss OR2M7 OR2L8 OR2M5 OR2T8 OR2M3 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 OR2T2 OR2T35 OR2T27 OR2L3 OR2AK2 OR2T33 OR2T3 OR2T34 OR2T1 OR2L1P OR2L13 OR2M4 OR2T5 OR2T10 OR2T12 OR2T11 OR2M2 OR2M1P OR2W3 OR2L5 OR14C36
nsv508707 Chr.1:248510229 - 248537834 on Build GRCh38 Deletion OR2T10 OR2G6
esv2750835 Chr.1:248359378 - 248864040 on Build GRCh38 Gain ZNF672 OR2T35 OR2T27 ZNF692 OR2T3 OR2T34 OR2T1 OR14I1 LOC101928226 OR2G6 OR2T29 OR2T4 OR2T5 OR2T10 OR2T11 SH3BP5L OR2T6 LYPD8 OR2T2 MIR3124
nsv1160483 Chr.1:248475325 - 248650779 on Build GRCh38 Duplication OR2T29 OR2T35 OR2T27 OR2T5 OR2T10 OR2T11 OR2T34 OR2G6
esv3891415 Chr.1:247876411 - 248795772 on Build GRCh38 Gain OR2M7 TRIM58 OR2L8 OR2M5 OR2T8 OR2M3 OR14I1 LOC101928226 OR2G6 OR2T29 OR2T4 OR2T6 OR2L2 LYPD8 OR2T2 OR2T35 OR2T27 OR2L3 OR2AK2 OR2T33 OR2T3 OR2T34 OR2T1 OR2L1P OR2L13 OR2M4 OR2T5 OR2T10 OR2T12 OR2T11 OR2M2 OR2M1P OR2W3 OR2L5 OR14C36
nsv1010059 Chr.1:248475313 - 248661824 on Build GRCh38 Loss OR2T29 OR2T35 OR2T27 OR2T5 OR2T10 OR2T11 OR2T34 OR2G6
esv2750832 Chr.1:247897657 - 248873491 on Build GRCh38 Gain OR2M7 OR2L8 OR2M5 OR2T8 OR2M3 OR14I1 LOC101928226 OR2G6 PGBD2 OR2T29 OR2T4 OR2T6 OR2L2 LYPD8 OR2T2 MIR3124 ZNF672 OR2T35 OR2T27 OR2L3 ZNF692 OR2AK2 OR2T33 OR2T3 OR2T34 OR2T1 OR2L1P OR2L13 OR2M4 OR2T5 OR2T10 OR2T12 OR2T11 OR2M2 OR2M1P SH3BP5L OR2L5 OR14C36
dgv20n17 Chr.1:248324336 - 248684068 on Build GRCh38 Loss OR2M7 OR2T35 OR2T27 OR2T3 OR2T34 OR2T1 OR14I1 OR2G6 OR2T29 OR2T4 OR2T5 OR2T10 OR2T11 OR2T6 OR14C36 OR2T2

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More Information


Additional Information:

For this assay, SNP(s) [rs73149450] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Non-exonic DGV Variation

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