ClinVar Miner

List of variants reported as likely pathogenic by ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 10q21.1(chr10:54991837-55295059)x1
GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972)x3
GRCh37/hg19 11p11.2(chr11:45873733-46409298)x1
GRCh37/hg19 11q14.1-21(chr11:84924674-93574799)x1
GRCh37/hg19 12p12.2-12.1(chr12:20837998-22734873)x3
GRCh37/hg19 12q23.2-24.11(chr12:103044333-111639805)x1
GRCh37/hg19 12q24.21(chr12:116374312-116535323)x3
GRCh37/hg19 12q24.23-24.31(chr12:118486842-120995382)x3
GRCh37/hg19 12q24.31-24.32(chr12:122726807-127365912)x1
GRCh37/hg19 13q11-12.11(chr13:19436286-20127438)x1
GRCh37/hg19 13q12.11(chr13:20523271-21972234)x1
GRCh37/hg19 13q13.3(chr13:35531798-39607778)x1
GRCh37/hg19 13q13.3(chr13:36064105-39230796)x1
GRCh37/hg19 13q14.2(chr13:49805984-50472203)x3
GRCh37/hg19 13q34(chr13:113625366-114153873)x1
GRCh37/hg19 14q32.2-32.33(chr14:98051841-107285437)x3
GRCh37/hg19 15q13.1-13.3(chr15:28659910-32446830)x4
GRCh37/hg19 15q13.1-13.3(chr15:28659910-32915593)x4
GRCh37/hg19 16p11.2(chr16:28802397-29084772)x3
GRCh37/hg19 16p12.2(chr16:21596299-21740200)x0
GRCh37/hg19 16p13.11(chr16:15054174-16327476)x3
GRCh37/hg19 16p13.11-12.3(chr16:15193982-18172468)x3
GRCh37/hg19 16p13.3(chr16:6351706-6383565)x1
GRCh37/hg19 18q21.2(chr18:53290008-53383013)x1
GRCh37/hg19 1p31.3(chr1:61604866-61847475)x1
GRCh37/hg19 1p34.1-32.3(chr1:45303358-52157856)x1
GRCh37/hg19 1q42.13(chr1:229555499-229577325)x1
GRCh37/hg19 1q44(chr1:244155894-244505317)x1
GRCh37/hg19 20p11.21-q11.21(chr20:24162775-31820857)x3
GRCh37/hg19 20p12.3(chr20:6296284-7092386)x1
GRCh37/hg19 20p13(chr20:61568-806878)x1
GRCh37/hg19 22q11.21(chr22:19024656-21465659)x3
GRCh37/hg19 22q11.22-11.23(chr22:22997802-25002659)x3
GRCh37/hg19 2q13(chr2:110504318-110980108)x1
GRCh37/hg19 2q13(chr2:111366255-113132395)x3
GRCh37/hg19 2q22.1-22.3(chr2:138578298-144874187)x1
GRCh37/hg19 2q23.3(chr2:150606201-153038451)x1
GRCh37/hg19 2q36.1-37.1(chr2:223378640-232061074)x1
GRCh37/hg19 2q37.1(chr2:232215111-235593473)x1
GRCh37/hg19 3p24.2-22.3(chr3:25045365-32691140)x1
GRCh37/hg19 4p15.2-15.1(chr4:23790131-32302608)x1
GRCh37/hg19 4q25-26(chr4:112857598-115434654)x1
GRCh37/hg19 5p15.33-15.31(chr5:1359855-7263257)x1
GRCh37/hg19 6p22.3(chr6:16348584-16559316)x1
GRCh37/hg19 6p24.3-22.3(chr6:8269414-17402660)x3
GRCh37/hg19 7p22.3-22.2(chr7:43360-2825753)x3
GRCh37/hg19 8p11.23-11.22(chr8:37566388-38802788)x1
GRCh37/hg19 8p23.1(chr8:9144943-11945856)x3
GRCh37/hg19 9p24.3-24.1(chr9:1232387-4611862)x1
GRCh37/hg19 Xp11.22(chrX:53797930-54608609)x3
GRCh37/hg19 Xp21.1(chrX:31881035-31993637)x1
GRCh37/hg19 Xq12-13.1(chrX:67570138-68576809)x3
GRCh37/hg19 Xq21.1(chrX:79898147-80011045)x2
GRCh37/hg19 Xq22.2-22.3(chrX:103046942-104214535)x0
GRCh37/hg19 Xq25(chrX:122838263-123455393)x2
GRCh37/hg19 Xq25-26.2(chrX:123108906-133026079)x3

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.