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Variant : CV248141 (GRCh37/hg19 7q22.1(chr7:99724620-99972850)x3) Homo sapiens

Symbol: CV248141
Name: GRCh37/hg19 7q22.1(chr7:99724620-99972850)x3
Condition: See cases [RCV000240398]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: GAL3ST4   GPC2   LAMTOR4   MAP11   MBLAC1   PILRA   PVRIG   SPDYE3   STAG3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37799,724,620 - 99,972,850CLINVAR
Cytogenetic Map77q22.1CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 11541801
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-07-07
Status: ACTIVE


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