ClinVar Miner

List of intergenic variants studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
2q13 deletion
46;X;inv(X)(p11.4q24)dn
46;X;t(X;5)(q24;q13)dn
46;XY;inv(6)(p22q13)dn
46;XY;t(12;14)(q15;q13)mat
46;XY;t(2;13)(p25.2;q31.3)dn
46;XY;t(6;12)(q14;q24);20p+dn
46;XY;t(8;9)(p11.2;q13)dn
46;Y;inv(X)(p11.2q28)mat
FGFR2-CLIP1 fusion
NC_000001.9:g.157610062_160185096del2575035
NC_000016.9:g.55493443_55496575del
NM_000784.3:c.10_11 ins10bp
NM_000784.3:c.1146_1151delins
NM_000784.3:c.1180-1181delCT
NM_000784.3:c.1263+81_1596+?del
NM_000784.3:c.1323C>T
NM_000784.3:c.1330-1333delTTCC
NM_000784.3:c.599C>T
NM_003611.2:c.441+65A>G

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