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Variant : CV673193 (GRCh37/hg19 7p14.1(chr7:38732592-38853944)x1) Homo sapiens

Symbol: CV673193
Name: GRCh37/hg19 7p14.1(chr7:38732592-38853944)x1
Condition: not provided [RCV000846309]
Clinical Significance: uncertain significance
Last Evaluated: 12/01/2017
Review Status: no assertion criteria provided
Related Genes: VPS41  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37738,732,592 - 38,853,944CLINVAR
Cytogenetic Map77p14.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976885
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-07
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.