ClinVar Miner

List of variants reported as uncertain significance by ISCA site 8

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Minimum conflict level:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 1q21.1(chr1:144451745-144524956)x1
GRCh38/hg38 10q11.23(chr10:49109413-49618870)x1
GRCh38/hg38 10q22.1(chr10:71169571-71556196)x1
GRCh38/hg38 11p15.4(chr11:2883714-2883812)x3
GRCh38/hg38 13q12.11(chr13:19503409-20005117)x3
GRCh38/hg38 13q12.11(chr13:19632400-20005117)x3
GRCh38/hg38 14q23.3(chr14:64952923-66295289)x3
GRCh38/hg38 15q11.2(chr15:22572809-23066575)x3
GRCh38/hg38 15q11.2(chr15:22726969-23066575)x1
GRCh38/hg38 15q11.2(chr15:22787972-23066575)x1
GRCh38/hg38 15q13.3(chr15:31729530-32218662)x3
GRCh38/hg38 15q13.3(chr15:31738809-32217725)x3
GRCh38/hg38 16p11.2(chr16:28589904-29030797)x3
GRCh38/hg38 16q23.3(chr16:82173150-83629769)x3
GRCh38/hg38 17p11.2(chr17:19744033-21598663)x3
GRCh38/hg38 17p11.2(chr17:21416753-22176920)x3
GRCh38/hg38 17p13.1(chr17:10145851-10464716)x3
GRCh38/hg38 17p13.3(chr17:2254635-2699329)x3
GRCh38/hg38 17p13.3(chr17:759449-999134)x3
GRCh38/hg38 17q12(chr17:35129859-35767049)x3
GRCh38/hg38 18p11.23(chr18:7438814-8412548)x3
GRCh38/hg38 1p13.3(chr1:108807502-109134584)x3
GRCh38/hg38 1p31.1(chr1:71592911-73610754)x3
GRCh38/hg38 2p14(chr2:67161296-67998206)x1
GRCh38/hg38 2p22.1(chr2:39054693-39369157)x3
GRCh38/hg38 2p25.3(chr2:39193-992648)x1
GRCh38/hg38 2q11.2(chr2:96100812-97154835)x1
GRCh38/hg38 4q13.3(chr4:74097483-75266770)x1
GRCh38/hg38 5q31.2(chr5:139103408-139683294)x3
GRCh38/hg38 6p23-22.3(chr6:14545345-16062792)x3
GRCh38/hg38 6q15-16.1(chr6:90888950-93582834)x1
GRCh38/hg38 6q16.1-16.2(chr6:98770647-99813111)x1
GRCh38/hg38 6q22.31(chr6:123352392-123845516)x3
GRCh38/hg38 8p23.1(chr8:12182421-12546553)x3
GRCh38/hg38 8p23.1(chr8:7411297-8222398)x3
GRCh38/hg38 Xp11.22(chrX:53403791-53795603)x2
GRCh38/hg38 Xq25(chrX:122217427-123074195)x2
GRCh38/hg38 Xq28(chrX:154904963-155331063)x1
GRCh38/hg38 Xq28(chrX:155227210-155331063)x2

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