ClinVar Miner

List of variants reported for Small for gestational age by Institute of Molecular and Cell Biology, University of Tartu

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Total variants: 61
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HGVS dbSNP gnomAD frequency
CM000664.1:g.154163944_154199490dup
CM000665.1:g.128391789_128412024dup
CM000665.1:g.162132155_162142475dup
CM000668.1:g.112955668_112968423dup
CM000671.1:g.30181745_30222006dup
CM000674.1:g.129226773_129266496dup
CM000676.1:g.90758891_90802050dup
GRCh37/hg19 3q25.1(chr3:151514590-151574286)x1
GRCh38/hg38 10q21.3(chr10:66318723-66354723)x1
NC_000001.10:g.50863202_50874830del
NC_000001.11:g.103611243_103613322del
NC_000001.11:g.2427505_2438059dup
NC_000001.11:g.73494196_73528121dup
NC_000002.12:g.240619519_240637209dup
NC_000003.12:g.163943745_163946498del
NC_000003.12:g.22241802_22244073del
NC_000003.12:g.62972896_63007409del
NC_000003.12:g.66534498_66579341dup
NC_000003.12:g.8788186_8816277dup
NC_000004.12:g.128853220_129006649dup
NC_000004.12:g.160140992_160149907del
NC_000004.12:g.161031076_161082472dup
NC_000004.12:g.35148038_35149615del
NC_000005.10:g.156050857_156057228del
NC_000006.12:g.147348950_147402441dup
NC_000007.14:g.109815648_109837120dup
NC_000007.14:g.147420362_147448484dup
NC_000007.14:g.53130576_53138532del
NC_000008.11:g.40327353_40332030del
NC_000008.11:g.5741878_5747566del
NC_000009.12:g.83588331_83591428del
NC_000010.11:g.44713993_44864035dup
NC_000011.10:g.104495361_104501590del
NC_000011.10:g.264391_396308dup
NC_000011.10:g.394005_419906dup
NC_000011.10:g.99506676_99703958dup
NC_000012.12:g.31106438_31253973dup
NC_000012.12:g.31113353_31253973dup
NC_000012.12:g.52452168_52466201del
NC_000014.9:g.90322590_90335706dup
NC_000015.10:g.85968459_85978252del
NC_000015.9:g.23077857_23114374del
NC_000016.10:g.31209548_31215370del
NC_000017.11:g.46092442_46290846dup
NC_000017.11:g.79371616_79400400dup
NC_000018.10:g.33322025_33429787dup
NC_000018.10:g.66241835_66245461del
NC_000021.9:g.22647904_22670749del
NM_001010848.3(NRG3):c.824-173790_824-159316del
NM_001040214.2(NKAIN2):c.55-187304_55-129556dup
NM_001277864.1(DHRS4L1):c.-23423_-119+7390del
NM_001282658.2(CCDC3):c.-1-19898_-1-16075del
NM_001320322.1(TMTC2):c.84-78853_84-44447del
NM_001363059.2(MTUS1):c.2288-795_2449+390del
NM_002125.3(HLA-DRB5):c.-21004_-833del
NM_002155.4(HSPA6):c.-1862_*5145del
NM_002353.2(TACSTD2):c.-43393_*17422del
NM_024090.2(ELOVL6):c.-68192_89+40066dup
NM_152721.6(DOK6):c.67-22582_67-14452del
NR_001317.3(HCG4B):n.-1429_25883del
Single allele

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