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          • Home
          • › Search Tool
          • › Search Results
          • › Hs01686656_cn
          See other BEND7 CNV Assays ›
          Gene Symbol
          BEND7
          Assay Reference Genome
          Location

          Chr.10:13496816 on build GRCh38
          Cytoband
          10p13
          Assay ID Hs01686656_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
          Your Price
          Online offer:
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          222389

          Gene Name:

          BEN domain containing 7

          Gene Aliases:

          C10orf30

          Location:

          Chr.10:13438484-13528772 on Build GRCh38

          Assay Gene Location:

          Overlaps Intron 7 - Exon 7
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          BEND7 NM_001100912.1 NP_001094382.1
          NM_152751.2 NP_689964.2
          XM_005252402.4 XP_005252459.1
          XM_011519390.2 XP_011517692.1
          XM_011519391.2 XP_011517693.1
          XM_011519392.2 XP_011517694.1
          XM_011519393.2 XP_011517695.1
          XM_011519394.2 XP_011517696.1
          XM_011519395.2 XP_011517697.1
          XM_011519396.2 XP_011517698.1
          XM_011519397.2 XP_011517699.1
          XM_011519398.2 XP_011517700.1
          XM_011519399.2 XP_011517701.1
          XM_011519400.2 XP_011517702.1
          XM_011519401.2 XP_011517703.1
          XM_011519402.2 XP_011517704.1
          XM_011519403.2 XP_011517705.1
          XM_011519404.2 XP_011517706.1
          XM_011519405.2 XP_011517707.1
          XM_011519406.2 XP_011517708.1
          XM_011519407.1 XP_011517709.1
          XM_011519408.2 XP_011517710.1
          XM_011519410.2 XP_011517712.1
          XM_011519411.2 XP_011517713.1
          XM_011519412.1 XP_011517714.1
          XM_011519413.1 XP_011517715.1
          XM_011519414.1 XP_011517716.1
          XM_017015915.1 XP_016871404.1
          XM_017015916.1 XP_016871405.1
          XM_017015917.1 XP_016871406.1
          XM_017015918.1 XP_016871407.1
          XM_017015919.1 XP_016871408.1
          AK097602.1 BAC05114.1
          BC031618.1 AAH31618.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv825252 Chr.10:13492728 - 13549437 on Build GRCh38 Gain BEND7
          esv1007603 Chr.10:13489372 - 13500710 on Build GRCh38 Deletion BEND7

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          More Information


          Set Membership:

          Intragenic Non-exonic DGV Variation

          Gene Ontology Categories:

          Process(es)

          protein binding

          Back To Top

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