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Variant : CV158801 (GRCh38/hg38 7q22.1(chr7:99932610-102473188)x3) Homo sapiens

Symbol: CV158801
Name: GRCh38/hg38 7q22.1(chr7:99932610-102473188)x3
Condition: See cases [RCV000138109]
Clinical Significance: uncertain significance
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC004522.6   ACHE   ACTL6B   AGFG2   ALKBH4   AP1S1   AP4M1   AZGP1   C7orf61   CLDN15   CNPY4   COL26A1   COPS6   CUX1   EMSLR   EPHB4   EPO   FBXO24   FIS1   GAL3ST4   GIGYF1   GNB2   GPC2   IFT22   LAMTOR4   LINC01007   LNCPRESS1   LRCH4   LRWD1   MAP11   MBLAC1   MCM7   MEPCE   MIR106B   MIR25   MIR4285   MIR4467   MIR4653   MIR4658   MIR5090   MIR548O   MIR6840   MIR6875   MIR93   MOGAT3   MOSPD3   MUC12   MUC12-AS1   MUC17   MUC3A   MYL10   NAT16   NYAP1   ORAI2   PCOLCE   PCOLCE-AS1   PILRA   PILRB   PLOD3   POLR2J   POP7   PPP1R35   PPP1R35-AS1   PRKRIP1   PVRIG   SAP25   SERPINE1   SH2B2   SLC12A9   SLC12A9-AS1   SPDYE3   SPDYE6   SRRT   STAG3   STAG3L5P-PVRIG2P-PILRB   TAF6   TFR2   TRIM56   TRIP6   TSC22D4   UFSP1   VGF   ZAN   ZCWPW1   ZKSCAN1   ZNF3   ZNHIT1   ZSCAN21  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_99932610)_(102473188_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38799,932,610 - 102,473,188CLINVAR
GRCh37799,530,233 - 102,113,635CLINVAR
Build 36799,368,169 - 101,900,640CLINVAR
Cytogenetic Map77q22.1CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9485658
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.