ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 10p12.31(chr10:19415355-19831439)x1
GRCh37/hg19 10q21.1(chr10:58942915-59281629)x1
GRCh37/hg19 10q21.1(chr10:58964671-59689830)x3
GRCh37/hg19 10q26.3(chr10:133147184-133677330)x3
GRCh37/hg19 11p14.3(chr11:23370182-24192836)x3
GRCh37/hg19 11q14.3(chr11:90139851-90697895)x1
GRCh37/hg19 13q11-12.11(chr13:19436286-19634794)x1
GRCh37/hg19 13q21.1(chr13:55521443-55988184)x1
GRCh37/hg19 13q21.2-21.31(chr13:62066630-62678674)x3
GRCh37/hg19 13q21.31(chr13:63993755-64995614)x3
GRCh37/hg19 13q21.33(chr13:69238141-69520384)x1
GRCh37/hg19 13q33.1(chr13:103924982-104547066)x3
GRCh37/hg19 18q12.3(chr18:37523158-38454618)x3
GRCh37/hg19 18q23(chr18:75276459-76557917)x3
GRCh37/hg19 1p21.1(chr1:106030627-106269061)x1
GRCh37/hg19 21q21.2(chr21:24064639-26619069)x1
GRCh37/hg19 21q21.2(chr21:24419322-25233336)x1
GRCh37/hg19 22q13.32-13.33(chr22:49396258-50003999)x3
GRCh37/hg19 2p12(chr2:78300997-78755847)x1
GRCh37/hg19 3p24.3(chr3:21902066-22149030)x1
GRCh37/hg19 3p26.1(chr3:6465310-6814988)x1
GRCh37/hg19 3q13.13(chr3:109068746-109485501)x1
GRCh37/hg19 4q26(chr4:116982101-117704797)x3
GRCh37/hg19 4q35.2(chr4:189069140-189760810)x1
GRCh37/hg19 4q35.2(chr4:189069140-189765784)x1
GRCh37/hg19 4q35.2(chr4:189183165-189887863)x3
GRCh37/hg19 4q35.2(chr4:189244446-189767847)x3
GRCh37/hg19 4q35.2(chr4:189390411-190541809)x3
GRCh37/hg19 4q35.2(chr4:189515297-190067636)x3
GRCh37/hg19 4q35.2(chr4:190317436-190659162)x1
GRCh37/hg19 5q21.1(chr5:100941733-101251362)x1
GRCh37/hg19 5q34(chr5:163341266-164172249)x3
GRCh37/hg19 6p11.2(chr6:57206541-58070622)x3
GRCh37/hg19 6p11.2(chr6:57212534-58070622)x3
GRCh37/hg19 6p11.2(chr6:57360339-58060394)x3
GRCh37/hg19 6q14.1(chr6:78349741-79021310)x3
GRCh37/hg19 7p21.1(chr7:19870306-20103888)x1
GRCh37/hg19 8p21.3(chr8:20271412-21031778)x3
GRCh37/hg19 9p21.1(chr9:30279168-30592305)x1
GRCh37/hg19 9p21.3(chr9:22641632-23034642)x1
GRCh37/hg19 Xp22.33(chrX:1717089-2247079)x3
GRCh37/hg19 Xp22.33(chrX:1734397-2449612)x3
GRCh38/hg38 15q21.1(chr15:46187987-46736754)x1
NCBI36/hg18 10q11.21-11.22(chr10:45970809-47172593)x1
NCBI36/hg18 11q14.1(chr11:83878188-84133804)x1
NCBI36/hg18 11q22.2(chr11:101948892-102308304)x1
NCBI36/hg18 12p12.3(chr12:15734965-15932800)x1
NCBI36/hg18 12q23.3(chr12:105753678-106472787)x3
NCBI36/hg18 12q24.33(chr12:130016326-130615592)x4
NCBI36/hg18 15q14(chr15:35917871-36365367)x3
NCBI36/hg18 17p12-11.2(chr17:15552419-16500266)x1
NCBI36/hg18 19q12(chr19:32545047-33498313)x3
NCBI36/hg18 1p11.1(chr1:122727790-122920857)x1
NCBI36/hg18 1p31.1(chr1:78976422-79245677)x1
NCBI36/hg18 1p36.32(chr1:3799753-4103369)x1
NCBI36/hg18 1q23.3(chr1:159103072-159482433)x3
NCBI36/hg18 1q42.3(chr1:233678809-234482130)x3
NCBI36/hg18 2q21.2(chr2:132435795-133072329)x3
NCBI36/hg18 2q22.1(chr2:137649322-137908808)x1
NCBI36/hg18 3q21.1(chr3:124601187-125247394)x3
NCBI36/hg18 4p15.31(chr4:20606600-21125713)x3
NCBI36/hg18 4p15.31(chr4:21212019-22031914)x3
NCBI36/hg18 4q31.3(chr4:151567351-151957231)x1
NCBI36/hg18 4q35.2(chr4:190348265-190635095)x1
NCBI36/hg18 5q14.2-14.3(chr5:82243098-83063511)x1
NCBI36/hg18 6q25.3(chr6:158513655-159086606)x3
NCBI36/hg18 7q21.13(chr7:88030801-89950219)x3
NCBI36/hg18 7q34(chr7:141673351-142374954)x3
NCBI36/hg18 7q36.1(chr7:147711471-148261233)x1
NCBI36/hg18 Xp22.2(chrX:12922557-13871573)x3
NCBI36/hg18 Xp22.33(chrX:1738816-2346346)x3
NCBI36/hg18 Xq11.1(chrX:63966322-64832797)x3
NCBI36/hg18 Yp11.2(chrY:6652868-7273772)x0

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