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          • Home
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          • › Hs03737413_cn
          Assay Reference Genome
          Location

          Chr.10:46108239 on build GRCh38
          Cytoband
          Assay ID Hs03737413_cn
          Size
          Availability Made To Order
          Catalog # 4400291
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          • Genomic Map
          • Assay Details
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          Genomic Map

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          Assay Details

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2025-12-01, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          nsv4186119 Chr.10:46107772 - 46120822 on Build GRCh38 Deletion AGAP7P
          nsv4178909 Chr.10:45987582 - 46118622 on Build GRCh38 Duplication AGAP7P MSMB TIMM23 NCOA4
          esv3577172 Chr.10:45959639 - 46146408 on Build GRCh38 Gain PARGP1-AGAP4 AGAP7P MSMB TIMM23 SNORA74C-1 NCOA4 PARGP1
          nsv6438829 Chr.10:46106523 - 46282986 on Build GRCh38 Deletion ANTXRLP1 AGAP7P
          nsv4176195 Chr.10:46089822 - 46121322 on Build GRCh38 Duplication AGAP7P
          nsv5927437 Chr.10:46099675 - 46274712 on Build GRCh38 Deletion ANTXRLP1 AGAP7P
          nsv5479995 Chr.10:46086265 - 46121265 on Build GRCh38 Duplication AGAP7P
          nsv4180598 Chr.10:46106672 - 46120872 on Build GRCh38 Duplication AGAP7P
          nsv4187632 Chr.10:45990335 - 46113822 on Build GRCh38 Deletion AGAP7P MSMB TIMM23 NCOA4
          nsv947992 Chr.10:46090524 - 46145248 on Build GRCh38 Duplication AGAP7P
          nsv5476351 Chr.10:46093785 - 46268341 on Build GRCh38 Deletion ANTXRLP1 AGAP7P
          nsv5489018 Chr.10:45680265 - 46362265 on Build GRCh38 Duplication AGAP14P AGAP4 AGAP7P LOC105378577 FAM25EP LOC107984227 WASHC2C AGAP10P PARGP1-AGAP4 ANTXRLP1 MSMB TIMM23 SNORA74C-1 ANTXRL NCOA4 PARGP1
          nsv508583 Chr.10:45881821 - 46146976 on Build GRCh38 Deletion PARGP1-AGAP4 AGAP7P MSMB TIMM23 SNORA74C-1 NCOA4 PARGP1
          nsv1042912 Chr.10:46009162 - 46116183 on Build GRCh38 Loss AGAP7P MSMB NCOA4
          esv22941 Chr.10:46090476 - 46146936 on Build GRCh38 Loss AGAP7P
          nsv5478574 Chr.10:46058265 - 46142265 on Build GRCh38 Duplication AGAP7P

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          More Information


          Additional Information:

          Set Membership:

          Intergenic/Unknown DGV Variation Validated

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