ClinVar Miner

List of intergenic variants reported as benign by ISCA site 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
GRCh37/hg19 Yq12(chrY:59002344-59031480)x2
GRCh38/hg38 14q21.1(chr14:40549523-40765447)x1
GRCh38/hg38 1q31.1(chr1:189362122-189543758)x1
GRCh38/hg38 2p22.3(chr2:35596740-35836838)x1
GRCh38/hg38 4q35.2(chr4:188915479-189171840)x3
GRCh38/hg38 4q35.2(chr4:188915538-189171840)x3
GRCh38/hg38 5p12(chr5:45858731-45880607)x1
GRCh38/hg38 5q21.1(chr5:101813186-102088050)x1
GRCh38/hg38 6p25.3(chr6:259318-289174)x1
GRCh38/hg38 6p25.3(chr6:259318-289174)x3
GRCh38/hg38 6p25.3(chr6:259881-283860)x1
GRCh38/hg38 6p25.3(chr6:259881-289174)x1
GRCh38/hg38 6p25.3(chr6:259881-289174)x3
GRCh38/hg38 6q27(chr6:170499112-170532540)x1
GRCh38/hg38 7p22.3(chr7:54185-120272)x3
GRCh38/hg38 7q36.3(chr7:159257125-159265304)x1
GRCh38/hg38 8q24.3(chr8:144972242-144997345)x1
GRCh38/hg38 Xq11.1(chrX:62712219-62928928)x3
GRCh38/hg38 Xq27.2(chrX:141258960-141469623)x0
GRCh38/hg38 Xq27.2(chrX:141258960-141469623)x2
GRCh38/hg38 Xq27.3(chrX:144251509-144488776)x2

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