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Variant : CV554592 (GRCh37/hg19 7p21.1-15.3(chr7:19173971-21399377)x3) Homo sapiens

Symbol: CV554592
Name: GRCh37/hg19 7p21.1-15.3(chr7:19173971-21399377)x3
Condition: not provided [RCV000682897]
Clinical Significance: uncertain significance
Last Evaluated: 08/24/2017
Review Status: no assertion criteria provided
Related Genes: ABCB5   FERD3L   ITGB8   MACC1   SP8   TMEM196   TWISTNB  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37719,173,971 - 21,399,377CLINVAR
Cytogenetic Map77p21.1-15.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13795798
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.