ClinVar Miner

List of intergenic variants reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000006.12:g.30806580G>A rs3130783 0.74896
NC_000006.12:g.43858890C>T rs943080 0.60993
NC_000015.10:g.58396268C>G rs920915 0.55380
NC_000016.10:g.56959412C>A rs3764261 0.31123
NC_000019.10:g.44919689A>G rs4420638 0.18374
NC_000008.11:g.104467074G>C rs78426610 0.03517
NC_000012.12:g.96000349G>T rs142926035 0.01088
NC_000017.11:g.7666228C>G rs144366923 0.00672
NR_163594.1(SSPO):n.13348A>C rs202144866 0.00473
NR_163193.1(TCP10):n.1018G>A rs140649985 0.00424
NR_163193.1(TCP10):n.943C>T rs200948850 0.00338
NR_163594.1(SSPO):n.15289G>A rs202079888 0.00183
NR_163594.1(SSPO):n.11109T>A rs200844215 0.00182
NC_000005.10:g.132556973G>A rs104895040 0.00001
CM000665.1:g.162132155_162142475dup
CM000666.1:g.161590091_161646978dup
CM000666.1:g.44976703_45002987dup
CM000668.1:g.112955668_112968423dup
CM000668.1:g.66593133_66622346dup
CM000670.1:g.84876695_84890104dup
CM000673.1:g.42151229_42185849dup
CM000675.1:g.81919202_81952150dup
CM000677.1:g.24594816_24668007dup
GRCh37/hg19 17p11.2(chr17:19515340-19536015)x1
GRCh38/hg38 5q15(chr5:97712762-97763616)x1
NCBI36/hg18 10p15.3-14(chr10:1-6889456)x1
NCBI36/hg18 16p11.2(chr16:29385560-30239515)x3
NCBI36/hg18 1q21.1(chr1:143639135-144458626)x3
NCBI36/hg18 1q41-44(chr1:214401568-247249719)
NCBI36/hg18 1q42.2(chr1:229779180-229879929)x3
NCBI36/hg18 2p25.3(chr2:1245633-1879818)x3
NCBI36/hg18 2p25.3(chr2:20341-2288046)x1
NCBI36/hg18 6p12.3(chr6:45579286-46089921)x3
NCBI36/hg18 7q11.22(chr7:69313697-69359559)x1
NCBI36/hg18 9p13.2(chr9:36470667-37047553)x3
NC_000001.10:g.(155160963_155162030)delinsAT
NC_000001.10:g.(155160963_155162030)dupGCCGGCCCCGGGTCC
NC_000001.10:g.(155160963_155162030)insC
NC_000001.10:g.(155160963_155162030)insG
NC_000001.10:g.50863202_50874830del
NC_000001.11:g.103611243_103613322del
NC_000001.11:g.111383531_111391682del
NC_000001.11:g.73494196_73528121dup
NC_000002.11:g.89427986_90240473dup
NC_000002.11:g.89427986_91820358dup
NC_000002.12:g.13346653_13396647dup
NC_000002.12:g.183933099_183937882del
NC_000002.12:g.49630800_49638002del
NC_000002.12:g.64468759_64476152del
NC_000002.12:g.76713923_76721975del
NC_000003.11:g.75428675_75469493del
NC_000003.12:g.128604048A>T rs1251296240
NC_000003.12:g.149246905_149249548del
NC_000003.12:g.151958534_151963230del
NC_000003.12:g.162413621_162421039del
NC_000003.12:g.163943745_163946498del
NC_000003.12:g.1740840_1742201del
NC_000003.12:g.28769097_28774591del
NC_000003.12:g.62972896_63007409del
NC_000003.12:g.65132272_65133087del rs1553673680
NC_000003.12:g.8788186_8816277dup
NC_000004.12:g.10396803_10398532del
NC_000004.12:g.121402957_121412610del
NC_000004.12:g.153660056_153664770del
NC_000004.12:g.160140992_160149907del
NC_000004.12:g.35148038_35149615del
NC_000004.12:g.45815310_45861251dup
NC_000004.12:g.65719204_65764047dup
NC_000005.10:g.177964050_177973551del
NC_000005.10:g.98598184_98603912del
NC_000006.12:g.128772127_128804039dup
NC_000006.12:g.19045329_19048542del
NC_000006.12:g.31253262_31261195del
NC_000006.12:g.31370751_31373580del
NC_000007.13:g.9636392_9847642del
NC_000007.14:g.109815648_109837120dup
NC_000007.14:g.146096986_146099665del
NC_000007.14:g.151893201_151902419del
NC_000007.14:g.19166813_19172086del
NC_000007.14:g.44935_63494dup
NC_000007.14:g.53130576_53138532del
NC_000007.14:g.62533792_63268846dup
NC_000008.11:g.16042179_16081673dup
NC_000008.11:g.16405000_16410993del
NC_000008.11:g.40327353_40332030del
NC_000008.11:g.5741877_5750141del
NC_000008.11:g.5741877_5750275del
NC_000008.11:g.5741877_5750560del
NC_000008.11:g.5741878_5747566del
NC_000008.11:g.5743669_5747565del
NC_000008.11:g.8725600_8730080del
NC_000008.11:g.95947591_95957128del
NC_000009.12:g.1447011_1450428del
NC_000010.11:g.36620136_36660204dup
NC_000010.11:g.76697830_76699453del
NC_000011.10:g.104495361_104501590del
NC_000011.10:g.17276557A>C rs186174
NC_000011.10:g.18114096_18116607del
NC_000011.10:g.34436683_34439157dup
NC_000011.10:g.34436683_34439164dup
NC_000011.10:g.37746927_37870122dup
NC_000012.12:g.128744329_128749559del
NC_000012.12:g.52452168_52466201del
NC_000013.10:g.90387429_90490883dup
NC_000013.11:g.103037119_103046863dup
NC_000013.11:g.22972099_22979379del
NC_000013.11:g.26440969_26443305del
NC_000013.11:g.58019523_58024897del
NC_000013.11:g.83214607_83217480del
NC_000013.11:g.83214607_83219840del
NC_000013.11:g.85294188_85330291dup
NC_000014.9:g.40385828_40389224del
NC_000015.10:g.23810341_23816350del
NC_000015.10:g.24361585_24422860dup
NC_000015.10:g.32217692_32222141dup
NC_000015.10:g.61395441_61400319del
NC_000015.10:g.81685124_81795773dup
NC_000015.10:g.85968459_85978252del
NC_000015.9:g.34760648_34800595del
NC_000016.10:g.28603922_28609431dup
NC_000017.11:g.19606768_19616131del
NC_000018.10:g.30235355_30236003del rs1555628672
NC_000018.10:g.65529212_65551550dup
NC_000018.10:g.66182443_66199550dup
NC_000018.10:g.66241835_66245461del
NC_000018.10:g.69080332_69088272del
NC_000020.11:g.7977119_7981425dup
NC_000021.9:g.22647904_22670749del
NC_012920.1(MT-CYB):m.263A>G rs2853515
NM_000249.3(MLH1):c.*281G>T rs104895003
NM_002125.3(HLA-DRB5):c.-21004_-833del
NR_046946.1(RNU6-81P):n.-14115_29574dup
NR_163594.1(SSPO):n.8646T>A rs747906568
NT_187614.1:g.363601_383924dup
Single allele

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.