ClinVar Miner

List of intergenic variants studied for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
10q21.3duplication
15q11.2-12duplication
15q13.3duplication
15q25.3duplication
16q24.1duplication
1q41 duplication
1q42.2deletion
20p12.1duplication
22q11.21deletion
2q14.3duplication
2q24.3deletion
2q37.3deletion
46;X;inv(X)(q27q28)
46;X;t(X;5)(p11.23;q35)dn
46;X;t(X;9)(p22.2;p13)dn
46;X;t(Y;16)(q11.23;p11.2);t(6;21)(p21.3;p13)dn
46;XX;inv(7)(q11.23q36.3)dn
46;XX;t(10;14)(p13;q21)dn
46;XX;t(19;21)(q13.3;q22.3)dn
46;XX;t(2;5)(q33;p15.3)
46;XX;t(4;13)(q31.3;q14.3)dn
46;XX;t(7;12)(q11.2;q12).ish
46;XX;t(9;19)(q22.3;q13.1)dn
46;XX;t(X;22)(q13;q13)
46;XY;ins(16;2)(q22.1;p16.2p21)pat
46;XY;inv(2)(q11.2q24.2)dn
46;XY;inv(7)(p15q34)mat
46;XY;t(11;19)(p11.2;p13.3)dn
46;XY;t(12;14)(q15;q13)mat
46;XY;t(1;10;4)(p32.2;q21.1;q23)dn
46;XY;t(1;12)(p32;p13)dn
46;XY;t(1;3)(p22;q21)dn
46;XY;t(1;6)(q23;q13)dn
46;XY;t(20;22)(q13.3;q11.2)
46;XY;t(2;11)(q31;q13.5)pat
46;XY;t(2;6)(q33;q21)dn
46;XY;t(3;18)(q13.31;q22.1)dn
46;XY;t(3;5)(q24;p15.3)dn
46;XY;t(4;14)(p15.32;q32.1)dn
46;XY;t(4;7)(q31;q22)dn
46;XY;t(5;15)(q11.2;q24)
46;XY;t(5;19)(q33;p13.1)dn
46;XY;t(5;7)(q14.3;q21.3)dn
46;XY;t(6;11)(q23;q21)or(q25;q21)dn
46;XY;t(7;12)(q21.13;q24)dn
46;XY;t(8;10)(q13;p13)dn
4q35.2deletion
5p15.31duplication
6p22.3duplication
6q23.3deletion
7q31.1duplication
7q31.32deletion
7q32.3duplication
7q35 duplication
8q24.13duplication
8q24.3duplication
9p24.1deletion
GRCh37/hg19 10q21.1(chr10:58932423-59272160)x1
GRCh37/hg19 Xp22.32(chrX:5073112-5578094)x1
GRCh37/hg19 Xp22.33(chrX:566009-1262195)x3
GRCh37/hg19 Xp22.33(chrX:566009-1356042)x3
GRCh37/hg19 Yp11.32(chrY:516009-1306042)x3
NCBI36/hg18 2p25.3(chr2:20341-2288046)x1
NCBI36/hg18 9q22.32-22.33(chr9:95946863-99986314)x1
NC_000002.10:g.146798229_150310317del
NM_005112.2(WDR1):c.4198C>T rs540561511
Single allele
chr17:g.(AC027266_AL353996)_(AC015726-AC087393)del
der(6)t(6;7)(p25.3;q32.3)
inv(X)(p22.2q28)

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