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Variant : CV434720 (GRCh37/hg19 7p14.1(chr7:38619347-40542932)x1) Homo sapiens

Symbol: CV434720
Name: GRCh37/hg19 7p14.1(chr7:38619347-40542932)x1
Condition: not provided [RCV000509377]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: AMPH   CDK13   MPLKIP   POU6F2   RALA   SUGCT   VPS41   YAE1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: phenotyping only
Position
Human AssemblyChrPosition (strand)Source
GRCh37738,619,347 - 40,542,932CLINVAR
Cytogenetic Map77p14.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13442597
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-21
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.