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Variant : CV437477 (GRCh37/hg19 7p15.3-14.3(chr7:24344104-28879357)x1) Homo sapiens

Symbol: CV437477
Name: GRCh37/hg19 7p15.3-14.3(chr7:24344104-28879357)x1
Condition: See cases [RCV000510695]
Clinical Significance: pathogenic
Last Evaluated: 05/22/2013
Review Status: no assertion criteria provided
Related Genes: C7orf31   CBX3   CREB5   CYCS   EVX1   GSDME   HIBADH   HNRNPA2B1   HOTAIRM1   HOTTIP   HOXA1   HOXA10   HOXA11   HOXA11-AS   HOXA13   HOXA2   HOXA3   HOXA4   HOXA5   HOXA6   HOXA7   HOXA9   JAZF1   LINC02860   MIR148A   MIR196B   MPP6   NFE2L3   NPVF   OSBPL3   SKAP2   SNX10   TAX1BP1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37724,344,104 - 28,879,357CLINVAR
Cytogenetic Map77p15.3-14.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443674
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.