ClinVar Miner

List of intergenic variants reported by ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories

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Gene type:
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Total variants: 26
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HGVS dbSNP
GRCh37/hg19 10q21.1(chr10:54991837-55295059)x1
GRCh37/hg19 12q14.1(chr12:59486648-59815610)x1
GRCh37/hg19 14q12(chr14:27367665-27520832)x1
GRCh37/hg19 14q31.1(chr14:79347141-79708660)x1
GRCh37/hg19 14q31.1(chr14:79406903-79550940)x1
GRCh37/hg19 15q26.2(chr15:95740003-96776696)x3
GRCh37/hg19 18q11.2(chr18:22207588-22290382)x1
GRCh37/hg19 1q21.2(chr1:147478432-147929323)x3
GRCh37/hg19 21q21.2(chr21:24509204-24821878)x1
GRCh37/hg19 22q13.32-13.33(chr22:49213316-49684418)x3
GRCh37/hg19 2p16.1(chr2:58768215-60030580)x3
GRCh37/hg19 4p15.1(chr4:32051792-35757406)x1
GRCh37/hg19 4p15.33(chr4:14879195-14950324)x1
GRCh37/hg19 4q28.3(chr4:135299250-137834481)x1
GRCh37/hg19 5p15.1(chr5:17640213-17717166)x1
GRCh37/hg19 7p22.1(chr7:6987699-7169005)x1
GRCh37/hg19 9q22.1(chr9:91341232-91497061)x1
GRCh37/hg19 Xp22.33(chrX:168546-372029)x3
GRCh37/hg19 Xp22.33(chrX:169921-2666411)x3
GRCh37/hg19 Xp22.33(chrX:540065-921582)x3
GRCh37/hg19 Xp22.33(chrX:602793-1262195)x3
GRCh38/hg38 14q21.1(chr14:39745754-40264866)x1
GRCh38/hg38 3q12.3(chr3:102762944-102958793)x1
GRCh38/hg38 5q21.2(chr5:104146369-104914103)x3
GRCh38/hg38 5q23.3(chr5:130198251-130757815)x1
GRCh38/hg38 Xq21.31(chrX:88829694-89621356)x1

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