ClinVar Miner

List of intergenic variants studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP
NC_000005.10:g.4478434A>C
NC_000006.12:g.135105435A>G rs4895441
NC_000007.14:g.67751383T>A
NC_000007.14:g.67763644A>G
NC_000007.14:g.67766270A>G
NC_000007.14:g.67768864T>C
NC_000007.14:g.67770265T>G
NC_000007.14:g.67770277A>G
NC_000007.14:g.67771556T>C
NC_000007.14:g.67772928A>C
NC_000011.10:g.121431110C>A
NC_000011.10:g.121431925T>A
NC_000011.10:g.121431937A>G
NC_000011.10:g.121432497G>A
NC_000011.10:g.121432865T>G
NC_000011.10:g.121435753G>A
NC_000011.10:g.56455965_56455966del
NC_000011.10:g.56673649T>C
NC_000011.10:g.56684041A>T
NC_000011.10:g.56685650G>T
NC_000011.10:g.56685847C>T
NC_000011.10:g.56686812G>A
NC_000011.10:g.56689664T>C
NC_000011.10:g.56693466_56693468del
NC_000011.10:g.56697829T>A
NC_000011.10:g.56698623C>T
NC_000011.10:g.56699609T>C
NC_000015.9:g.952_952delC
NC_000016.10:g.173755A>T rs2261869
NC_000016.10:g.177596T>G rs930009344
NC_000016.10:g.177603A>T rs545195355
NC_000016.10:g.177647G>A rs114920844
NC_000016.10:g.177694A>G rs76462751
NC_000017.11:g.19754534C>G
NC_000017.11:g.41535537G>A
NC_000017.11:g.41539026C>T
NC_000018.10:g.22148844T>A
NC_000018.10:g.22148845C>A
NC_000023.11:g.103181712T>C rs12854542
NC_000023.11:g.103181775C>G rs746040794
NC_000023.11:g.136644791A>G rs3092952
Single allele rs144366923
t(10;14)(p14;q24)dn
t(15;16)(q24;p13)dn
t(1;14)(q25;q11)dn
t(2;14)(p11.2;q11.2)dn
t(6;18)(q14.1;q21.1)dn
t(9;21)(p21;q22)dn

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