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Variant : CV164402 (GRCh38/hg38 7q22.1(chr7:99880388-100288453)x3) Homo sapiens

Symbol: CV164402
Name: GRCh38/hg38 7q22.1(chr7:99880388-100288453)x3
Condition: See cases [RCV000142715]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AP4M1   AZGP1   CASTOR3   CNPY4   COPS6   GAL3ST4   GJC3   GPC2   LAMTOR4   MAP11   MBLAC1   MCM7   MIR106B   MIR25   MIR4658   MIR93   PVRIG   STAG3   TAF6   TRIM4   ZKSCAN1   ZNF3   ZSCAN21  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_99880388)_(100288453_?)dup
NC_000007.13:g.(?_99478011)_(99886076_?)dup
NC_000007.12:g.(?_99315947)_(99724012_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38799,880,388 - 100,288,453CLINVAR
GRCh37799,478,011 - 99,886,076CLINVAR
Build 36799,315,947 - 99,724,012CLINVAR
Cytogenetic Map77q22.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490313
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE



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