ClinVar Miner

List of intergenic variants reported as benign by Department of Biotechnology,Institute of Molecular and Cell Biology, University of Tartu

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 11p11.12(chr11:50023832-50682188)x3
GRCh37/hg19 12q11(chr12:36702406-37120187)x3
GRCh37/hg19 12q12(chr12:38416139-38653605)x3
GRCh37/hg19 13q21.32(chr13:66172692-66345298)x3
GRCh37/hg19 13q21.32(chr13:68194708-68272196)x3
GRCh37/hg19 13q31.3(chr13:90387808-90490883)x3
GRCh37/hg19 13q34(chr13:111676920-111746149)x3
GRCh37/hg19 14q21.3(chr14:49463484-49657524)x3
GRCh37/hg19 17p11.2(chr17:21539613-21874036)x1
GRCh37/hg19 17q25.3(chr17:77365534-77394037)x3
GRCh37/hg19 18q22.1(chr18:65274155-65597947)x3
GRCh37/hg19 1p11.2(chr1:121171208-121289118)x3
GRCh37/hg19 1p21.1(chr1:103908591-104012569)x3
GRCh37/hg19 2p11.2(chr2:90010895-90240473)x3
GRCh37/hg19 2p16.3(chr2:51572556-51729681)x3
GRCh37/hg19 2q14.3(chr2:124069523-124251487)x3
GRCh37/hg19 3p26.1(chr3:6224872-6598777)x3
GRCh37/hg19 4p15.31(chr4:18303100-18412600)x3
GRCh37/hg19 4q28.1(chr4:127037075-127760876)x3
GRCh37/hg19 4q28.3(chr4:131965131-132354287)x3
GRCh37/hg19 5q23.3(chr5:129648250-130330467)x3
GRCh37/hg19 6q16.1(chr6:95354276-95676106)x3
GRCh37/hg19 6q23.3(chr6:137941485-138002056)x3
GRCh37/hg19 7p21.1(chr7:17584021-17640215)x3
GRCh37/hg19 7p21.3(chr7:13193276-13244473)x3
GRCh37/hg19 7p22.3(chr7:132529-162448)x3
GRCh37/hg19 7p22.3(chr7:37445-68920)x3
GRCh37/hg19 7q11.21(chr7:62043624-62336389)x3
GRCh37/hg19 7q11.23(chr7:76289033-76476970)x3
GRCh37/hg19 7q11.23(chr7:76432653-76476970)x3
GRCh37/hg19 9q31.1(chr9:104819532-104883836)x3
GRCh37/hg19 Xp22.11(chrX:22818110-22862852)x3
GRCh37/hg19 Xp22.31(chrX:6497085-6596639)x3
GRCh38/hg38 10q11.22(chr10:46172088-46275517)x1
GRCh38/hg38 10q25.1(chr10:105858290-105922247)x1
GRCh38/hg38 11p11.2-11.12(chr11:48497341-48921229)x1
GRCh38/hg38 11q12.1(chr11:56357174-56358386)x1
GRCh38/hg38 12q21.1(chr12:72849677-72970178)x1
GRCh38/hg38 14q21.2(chr14:43781886-43815123)x1
GRCh38/hg38 16p13.12(chr16:12595039-12636793)x1
GRCh38/hg38 18p11.32(chr18:1715757-1833681)x1
GRCh38/hg38 18p11.32(chr18:1898847-1963416)x1
GRCh38/hg38 1p21.1(chr1:102207943-102378169)x1
GRCh38/hg38 2p22.3(chr2:35173390-35441810)x1
GRCh38/hg38 2p22.3(chr2:35594620-35862576)x1
GRCh38/hg38 2q14.3(chr2:123484951-123548571)x1
GRCh38/hg38 3p24.2(chr3:25979874-26080352)x1
GRCh38/hg38 5q14.3(chr5:85091086-85248046)x1
GRCh38/hg38 5q15(chr5:97188217-97327643)x1
GRCh38/hg38 5q15(chr5:97712762-97763616)x1
GRCh38/hg38 6q14.1(chr6:78263214-78319651)x0
GRCh38/hg38 6q14.1(chr6:78319932-78376369)x0
GRCh38/hg38 7q11.23(chr7:76659716-76927895)x1
GRCh38/hg38 8p23.1(chr8:8467939-8587382)x1
GRCh38/hg38 9p23(chr9:11660141-11890047)x1
GRCh38/hg38 9q31.1(chr9:101832517-102089791)x1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.