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Variant : CV164232 (GRCh38/hg38 7p11.2(chr7:55733060-56107195)x1) Homo sapiens

Symbol: CV164232
Name: GRCh38/hg38 7p11.2(chr7:55733060-56107195)x1
Condition: See cases [RCV000142545]
Clinical Significance: benign
Last Evaluated: 07/30/2009
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CCT6A   CHCHD2   FRA7A   MRPS17   NIPSNAP2   PHKG1   PSPH   SEPTIN14   SNORA15   SNORA22B   SUMF2   ZNF713  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_55733060)_(56107195_?)del
NC_000007.13:g.(?_55800753)_(56174888_?)del
NC_000007.12:g.(?_55768247)_(56142382_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38755,733,060 - 56,107,195CLINVAR
GRCh37755,800,753 - 56,174,888CLINVAR
Build 36755,768,247 - 56,142,382CLINVAR
Cytogenetic Map77p11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9490143
Created: 2014-09-09
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.