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Variant : CV614063 (GRCh37/hg19 17q24.3-25.1(chr17:70720436-73175266)) Homo sapiens

Symbol: CV614063
Name: GRCh37/hg19 17q24.3-25.1(chr17:70720436-73175266)
Condition: not provided [RCV000767767]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: ARMC7   ATP5PD   BTBD17   C17orf77   C17orf80   CD300A   CD300C   CD300E   CD300LB   CD300LD   CD300LF   CDC42EP4   CDR2L   COG1   CPSF4L   DNAI2   FADS6   FAM104A   FDXR   GPR142   GPRC5C   GRIN2C   HID1   JPT1   KCTD2   KIF19   MRPL58   NAT9   NT5C   OTOP2   OTOP3   RAB37   RPL38   SDK2   SLC16A5   SLC39A11   SLC9A3R1   SSTR2   SUMO2   TMEM104   TTYH2   USH1G  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371770,720,436 - 73,175,266CLINVAR
Cytogenetic Map1717q24.3-25.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14399719
Created: 2019-05-07
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.