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Variant : CV380877 (GRCh37/hg19 17q25.1(chr17:71940807-72667784)x3) Homo sapiens

Symbol: CV380877
Name: GRCh37/hg19 17q25.1(chr17:71940807-72667784)x3
Condition: See cases [RCV000445893]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: BTBD17   C17orf77   CD300A   CD300C   CD300E   CD300LB   CD300LD   DNAI2   GPR142   GPRC5C   KIF19   RAB37   RPL38   TTYH2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371771,940,807 - 72,667,784CLINVAR
Cytogenetic Map1717q25.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12850623
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-31
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.