ClinVar Miner

List of intergenic variants reported by ISCA site 8

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
GRCh37/hg19 10q11.22(chr10:47006954-47074861)x1
GRCh37/hg19 1q21.1(chr1:144451745-144524956)x1
GRCh37/hg19 1q21.1(chr1:144451745-144524956)x3
GRCh37/hg19 Yq12(chrY:59002344-59031480)x2
GRCh38/hg38 10q26.3(chr10:133577759-133597879)x3
GRCh38/hg38 12q24.32(chr12:126162882-126309883)x1
GRCh38/hg38 14q21.2(chr14:45352239-45510526)x1
GRCh38/hg38 16p13.11(chr16:16431432-16678513)x1
GRCh38/hg38 1q31.1(chr1:188236818-188605371)x1
GRCh38/hg38 1q31.1(chr1:189160201-189955259)x3
GRCh38/hg38 1q31.1(chr1:189362122-189543758)x1
GRCh38/hg38 1q31.1(chr1:189460972-189593144)x1
GRCh38/hg38 1q31.3(chr1:194809903-195658107)x3
GRCh38/hg38 1q31.3(chr1:195293008-195379302)x1
GRCh38/hg38 2p21(chr2:44004254-44049785)x1
GRCh38/hg38 3p12.3(chr3:74979514-75115565)x1
GRCh38/hg38 4q26(chr4:115400193-115992597)x1
GRCh38/hg38 5q31.3(chr5:144648025-144858721)x1
GRCh38/hg38 7p14.1(chr7:41184839-41403900)x1
GRCh38/hg38 7q31.31(chr7:119226617-119374558)x1
GRCh38/hg38 8p11.22(chr8:39401375-39528639)x0
GRCh38/hg38 8p11.22(chr8:39401375-39528639)x3
GRCh38/hg38 8q11.1(chr8:46031334-46662449)x1
GRCh38/hg38 9p23(chr9:12031727-12114297)x1
GRCh38/hg38 Xp22.31(chrX:7515855-7666651)x2
GRCh38/hg38 Xq11.1(chrX:62779286-62913742)x2
GRCh38/hg38 Xq25(chrX:122217427-123074195)x2
NCBI36/hg18 1q21.1(chr1:142444242-142683157)x1
NCBI36/hg18 7q11.23(chr7:74381487-74594440)x3

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