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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096310copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,097,373-39,306,081 , GRCh38.p12 chr22: 37,701,366-38,910,076 TMEM184B, ANKRD54, 46 more genes
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7037654copy number variation1nstd229human GRCh38 chr22: 38,831,701-38,835,600 , GRCh37.p13 chr22: 39,227,706-39,231,605 NPTXR
    nsv7036842copy number variation1nstd229human GRCh38 chr22: 38,813,468-38,839,088 , GRCh37.p13 chr22: 39,209,473-39,235,093 NPTXR
    nsv7036436copy number variation1nstd229human GRCh38 chr22: 38,834,073-38,834,127 , GRCh37.p13 chr22: 39,230,078-39,230,132 NPTXR
    nsv7035553copy number variation1nstd229human GRCh38 chr22: 38,831,650-38,835,650 , GRCh37.p13 chr22: 39,227,655-39,231,655 NPTXR
    nsv7022397copy number variation1nstd229human GRCh38 chr22: 38,815,945-38,836,997 , GRCh37.p13 chr22: 39,211,950-39,233,002 NPTXR
    nsv6552123copy number variation1nstd223human GRCh38 chr22: 38,815,945-38,836,995 , GRCh37.p13 chr22: 39,211,950-39,233,000 NPTXR
    nsv6551323copy number variation1nstd223human GRCh38 chr22: 38,831,650-38,835,646 , GRCh37.p13 chr22: 39,227,655-39,231,651 NPTXR
    nsv6547039copy number variation1nstd223human GRCh38 chr22: 38,840,601-38,843,300 , GRCh37.p13 chr22: 39,236,606-39,239,305 NPTXR
    nsv6542365copy number variation1nstd223human GRCh38 chr22: 38,806,398-38,816,936 , GRCh37.p13 chr22: 39,202,403-39,212,941 NPTXR
    nsv6538003copy number variation1nstd223human GRCh38 chr22: 38,814,170-38,821,151 , GRCh37.p13 chr22: 39,210,175-39,217,156 NPTXR
    nsv6226334copy number variation1nstd214human GRCh38 chr22: 38,834,073-38,834,126 , GRCh37.p13 chr22: 39,230,078-39,230,131 NPTXR
    nsv6134588copy number variation1nstd213human GRCh37 chr22: 38,630,000-39,360,001 , GRCh38.p12 chr22: 38,233,994-38,963,996 CSNK1E, KCNJ4, 24 more genes
    nsv6134213copy number variation1nstd213human GRCh37 chr22: 37,470,000-39,980,001 , GRCh38.p12 chr22: 37,073,960-39,583,996 ATF4, COX5BP7, 98 more genes
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