ClinVar Miner

List of intergenic variants reported as likely pathogenic by ISCA site 1

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
GRCh37/hg19 14q24.3-31.1(chr14:79293058-79466714)x1
GRCh37/hg19 1p36.22(chr1:9444639-9502799)x1
NCBI36/hg18 10p15.3(chr10:106418-1791937)x3
NCBI36/hg18 10q26.13-26.3(chr10:126994683-131957921)x1
NCBI36/hg18 11q13.3(chr11:70496451-70581405)x1
NCBI36/hg18 16q24.2(chr16:85907310-86380860)x1
NCBI36/hg18 2q11.2(chr2:96094786-97572638)x1
NCBI36/hg18 2q32.3-33.1(chr2:195941520-200787299)x1
NCBI36/hg18 4q21.22-21.3(chr4:83538638-87767627)x1
NCBI36/hg18 4q34.3-35.1(chr4:180056301-185397737)x3
NCBI36/hg18 5q31.2-32(chr5:138306445-143964773)x3
NCBI36/hg18 6q14.1-14.3(chr6:79678455-84862865)x1
NCBI36/hg18 6q16.1-16.3(chr6:97691375-103286627)x3
NCBI36/hg18 8q24.12(chr8:119981124-120831431)x1
NCBI36/hg18 8q24.13(chr8:125595512-126883514)x1

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