ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP
GRCh37/hg19 10q26.2(chr10:128328611-128544207)
GRCh37/hg19 11p14.3(chr11:21836986-22032466)
GRCh37/hg19 12q21.31(chr12:83765377-84013252)
GRCh37/hg19 12q24.32(chr12:127488730-127837052)
GRCh37/hg19 13q12.11(chr13:19612306-19679872)
GRCh37/hg19 13q12.11(chr13:22688792-22981935)
GRCh37/hg19 13q21.31(chr13:64295459-64400173)
GRCh37/hg19 13q31.1(chr13:85909019-86064348)
GRCh37/hg19 17p11.2(chr17:17316541-17349835)
GRCh37/hg19 2p12(chr2:78306103-78697833)
GRCh37/hg19 2p16.1(chr2:56277274-56381718)
GRCh37/hg19 3p12.1(chr3:86387381-86615770)
GRCh37/hg19 3p14.1(chr3:64992802-65051455)
GRCh37/hg19 3p14.1(chr3:64993928-65024494)
GRCh37/hg19 3p14.2(chr3:62955270-62998884)
GRCh37/hg19 5p14.1(chr5:25017057-25426009)
GRCh37/hg19 5q23.1(chr5:120513455-120921346)
GRCh37/hg19 5q31.1(chr5:131145181-131266601)
GRCh37/hg19 6q23.2(chr6:134730991-135020544)
GRCh37/hg19 7p22.1(chr7:6123758-6139997)
GRCh37/hg19 Xp22.2(chrX:13354873-13493086)
GRCh37/hg19 Xp22.33(chrX:1427577-1592679)
GRCh37/hg19 Xp22.33(chrX:2059627-2314248)
GRCh37/hg19 Xp22.33(chrX:370599-612414)
GRCh37/hg19 Xp22.33(chrX:417624-636092)
GRCh37/hg19 Xp22.33(chrX:426736-1215426)
GRCh37/hg19 Xp22.33(chrX:636950-820594)
GRCh37/hg19 Xq28(chrX:154873222-155010594)

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