ClinVar Miner

List of intergenic variants reported as uncertain significance by Clinical Genetics, Erasmus University Medical Center

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 13q12.11(chr13:22688792-22981935)
GRCh37/hg19 3p14.1(chr3:64992802-65051455)
NC_000002.11:g.102658576_102847088dup
NC_000003.12:g.146056770_146083362dup
NC_000018.10:g.48229615_48261302dup
NC_000018.10:g.6454094_6548625dup
NC_000023.11:g.3266860_3322912dup
NC_000023.11:g.95154038_95191395del

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