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Variant : CV156076 (GRCh38/hg38 7q22.1(chr7:99195836-100348063)x3) Homo sapiens

Symbol: CV156076
Name: GRCh38/hg38 7q22.1(chr7:99195836-100348063)x3
Condition: See cases [RCV000135630]
Clinical Significance: likely benign
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC004522.6   AP4M1   ARPC1A   ARPC1B   ATP5MF   ATP5MF-PTCD1   AZGP1   BUD31   CNPY4   COPS6   CPSF4   CYP3A4   CYP3A43   CYP3A5   CYP3A7   CYP3A7-CYP3A51P   FAM200A   GAL3ST4   GJC3   GPC2   KPNA7   LAMTOR4   MAP11   MBLAC1   MCM7   MIR106B   MIR12119   MIR25   MIR4658   MIR93   OR2AE1   PDAP1   PTCD1   PVRIG   SPDYE3   STAG3   STAG3L5P-PVRIG2P-PILRB   TAF6   TMEM225B   TRIM4   TRW-CCA5-1   ZKSCAN1   ZKSCAN5   ZNF3   ZNF394   ZNF655   ZNF789   ZSCAN21   ZSCAN25  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_99195836)_(100348063_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38799,195,836 - 100,348,063CLINVAR
GRCh37798,793,459 - 99,945,686CLINVAR
Build 36798,631,395 - 99,783,622CLINVAR
Cytogenetic Map77q22.1CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9483202
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.