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Variant : CV601618 (GRCh37/hg19 7q22.1(chr7:100141861-100552714)x1) Homo sapiens

Symbol: CV601618
Name: GRCh37/hg19 7q22.1(chr7:100141861-100552714)x1
Condition: not provided [RCV000746918]
Clinical Significance: likely benign
Last Evaluated: 10/22/2013
Review Status: no assertion criteria provided
Related Genes: ACHE   ACTL6B   AGFG2   EPHB4   EPO   FBXO24   GIGYF1   GNB2   LRCH4   MOSPD3   MUC3A   PCOLCE   POP7   SAP25   SLC12A9   SRRT   TFR2   TRIP6   UFSP1   ZAN  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh377100,141,861 - 100,552,714CLINVAR
Cytogenetic Map77q22.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14362265
Created: 2019-02-12
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.