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Variant : CV248206 (GRCh37/hg19 7p11.2(chr7:55874737-56172217)x1) Homo sapiens

Symbol: CV248206
Name: GRCh37/hg19 7p11.2(chr7:55874737-56172217)x1
Condition: See cases [RCV000239822]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: CCT6A   CHCHD2   MRPS17   NIPSNAP2   PHKG1   PSPH   SEPTIN14   SUMF2   ZNF713  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37755,874,737 - 56,172,217CLINVAR
Cytogenetic Map77p11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11541330
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-05-12
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.