ClinVar Miner

List of intergenic variants reported by Geisinger Autism and Developmental Medicine Institute,Geisinger Health System

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NC_000001.9:g.157610062_160185096del2575035
NC_000001.9:g.60109298_62267615del2158318
NC_000002.10:g.50979873_51700582del720710
NC_000003.10:g.113666631_116975648del3309018
NC_000003.10:g.186044109_188661490dup
NC_000003.10:g.85769721_87700993del1931273
NC_000004.10:g.147287237_191133858dup
NC_000004.10:g.33860_803885del770026
NC_000004.10:g.39249729_39994730dup
NC_000006.10:g.2922148_3317548dup
NC_000007.12:g.69828223_69859679del31457
NC_000008.9:g.16490154_17237631dup
NC_000009.10:g.194090_322539del128450
NC_000009.10:g.194090_406321del212232
NC_000009.10:g.449131_24197892dup
NC_000010.9:g.135104028_135284168del180141
NC_000010.9:g.75769258_77642312del1873055
NC_000013.9:g.113976035_114077122dup
NC_000013.9:g.31818484_31977333del158850
NC_000013.9:g.94652853_98706628dup
NC_000016.8:g.6936021_7063205del127185
NC_000016.8:g.7278231_7345380del67150
NC_000022.9:g.19075762_19790658del714897
NC_000022.9:g.28007909_28604388dup
NC_000023.10:g.614422_1238301dup
NC_000023.9:g.1131507_1713118dup
NC_000023.9:g.152940864_153059294dup
NC_000024.9:g.231527_536116dup
Single allele

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