ClinVar Miner

List of intergenic variants reported by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP
GRCh37/hg19 11q21(chr11:96458493-96808648)x1
GRCh37/hg19 12p12.3(chr12:16538820-16657476)x1
GRCh37/hg19 12q21.1(chr12:73145830-74392774)x1
GRCh37/hg19 13q31.1(chr13:85956080-86295850)x1
GRCh37/hg19 14q21.1(chr14:43026044-43222758)x1
GRCh37/hg19 14q23.2(chr14:62805750-62932251)x1
GRCh37/hg19 14q31.1(chr14:79535540-79637897)x1
GRCh37/hg19 15q26.3(chr15:100388548-100492097)x1
GRCh37/hg19 16p11.2(chr16:33462958-33625989)x1
GRCh37/hg19 16p13.2(chr16:8076862-8431175)x1
GRCh37/hg19 18q23(chr18:75788934-76138412)x3
GRCh37/hg19 19q13.42(chr19:53793603-53824343)x3
GRCh37/hg19 20q11.23(chr20:34959766-34960308)x1
GRCh37/hg19 20q13.33(chr20:59394373-59538047)x1
GRCh37/hg19 2p16.3(chr2:51968611-52200051)x3
GRCh37/hg19 2p22.3(chr2:36461440-36529829)x1
GRCh37/hg19 2q22.1(chr2:140075910-140320983)x3
GRCh37/hg19 2q22.1(chr2:140719548-140773999)x1
GRCh37/hg19 2q24.1(chr2:156151993-156272325)x1
GRCh37/hg19 2q24.1(chr2:156151993-156272325)x3
GRCh37/hg19 2q32.1(chr2:186534099-186590172)x1
GRCh37/hg19 3p26.1(chr3:4070291-4144113)x3
GRCh37/hg19 3p26.1(chr3:4094267-4144113)x3
GRCh37/hg19 3p26.3(chr3:1515856-1840338)x3
GRCh37/hg19 4p15.1(chr4:29339396-29700244)x1
GRCh37/hg19 4q13.1(chr4:64669283-64910669)x1
GRCh37/hg19 4q28.3(chr4:137155169-137267423)x1
GRCh37/hg19 4q32.1(chr4:158452579-158572531)x1
GRCh37/hg19 4q34.3(chr4:179738779-180001540)x3
GRCh37/hg19 5p15.2(chr5:12614302-12734149)x3
GRCh37/hg19 5p15.32(chr5:5500022-5663064)x3
GRCh37/hg19 5q13.2(chr5:69408016-69408880)x4
GRCh37/hg19 5q21.1(chr5:99597236-99760850)x1
GRCh37/hg19 5q21.1(chr5:99636546-99802449)x1
GRCh37/hg19 5q21.3-22.1(chr5:109476871-109635729)x1
GRCh37/hg19 6p11.2(chr6:57246930-58055076)x3
GRCh37/hg19 6q12(chr6:66418220-66536131)x1
GRCh37/hg19 6q14.3(chr6:85798377-86004117)x1
GRCh37/hg19 6q16.3(chr6:102804435-102915748)x1
GRCh37/hg19 6q26-27(chr6:164096437-164849627)x3
GRCh37/hg19 7p21.3(chr7:9271055-9472873)x1
GRCh37/hg19 7p21.3(chr7:9593631-9652744)x1
GRCh37/hg19 7p21.3(chr7:9614342-9758152)x0
GRCh37/hg19 7p21.3(chr7:9746919-10468761)x3
GRCh37/hg19 7q31.33(chr7:124607233-124712246)x1
GRCh37/hg19 8p21.2(chr8:25525483-25587783)x1
GRCh37/hg19 8p23.2(chr8:2256252-2349935)x3
GRCh37/hg19 8p23.3(chr8:812276-813543)x1
GRCh37/hg19 9p21.2(chr9:26274518-26372379)x1
GRCh37/hg19 9q31.1(chr9:105295810-105464481)x1
GRCh37/hg19 9q31.1(chr9:106362498-106760381)x1
GRCh37/hg19 Xp21.1(chrX:33897006-34008788)x1
GRCh37/hg19 Xp21.3(chrX:26525715-26812705)x3
GRCh37/hg19 Xp22.33(chrX:1213377-1793539)x3
GRCh37/hg19 Xp22.33(chrX:1728730-1906143)x2
GRCh37/hg19 Xp22.33(chrX:2052936-2170438)x2
GRCh37/hg19 Xq13.3(chrX:74772380-74826319)x1
GRCh37/hg19 Xq21.33(chrX:93622826-93916945)x1
GRCh37/hg19 Xq24(chrX:120600229-120697798)x0
GRCh37/hg19 Xq26.2(chrX:130684464-130960617)x3
GRCh37/hg19 Xq28(chrX:154947952-155207239)x2
NM_001024452.2(GLRA4):c.653C>T (p.Thr218Ile) rs759582026

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