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Items: 1 to 20 of 105

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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
    nsv7035511copy number variation1nstd229human GRCh38 chr22: 38,775,145-38,779,723 , GRCh37.p13 chr22: 39,171,150-39,175,728 DNAL4
    nsv7023030copy number variation1nstd229human GRCh38 chr22: 38,782,604-38,795,868 , GRCh37.p13 chr22: 39,178,609-39,191,873 DNAL4
    nsv6550294copy number variation1nstd223human GRCh38 chr22: 38,793,801-38,794,300 , GRCh37.p13 chr22: 39,189,806-39,190,305 DNAL4
    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
    nsv6134212copy number variation1nstd213human GRCh37 chr22: 36,430,000-39,960,001 , GRCh38.p12 chr22: 36,033,952-39,563,996 ATF4, COX5BP7, 133 more genes
    nsv5667377insertion1nstd207human GRCh38 chr22: 38,783,336-38,783,336 , GRCh37.p13 chr22: 39,179,341-39,179,341 DNAL4
    nsv5553601insertion1nstd206human GRCh38 chr22: 38,786,586-38,786,624 , GRCh37.p13 chr22: 39,182,591-39,182,629 DNAL4
    nsv5326903copy number variation1nstd204human GRCh38.p13 chr22: 38,792,395-38,803,345 , GRCh37.p13 chr22: 39,188,400-39,199,350 DNAL4
    nsv5326324copy number variation1nstd204human GRCh38.p13 chr22: 38,791,845-38,791,996 , GRCh37.p13 chr22: 39,187,850-39,188,001 DNAL4
    nsv5298475copy number variation1nstd204human GRCh38.p13 chr22: 38,792,551-38,793,850 , GRCh37.p13 chr22: 39,188,556-39,189,855 DNAL4
    nsv5295091copy number variation1nstd204human GRCh38.p13 chr22: 38,793,708-38,802,155 , GRCh37.p13 chr22: 39,189,713-39,198,160 DNAL4
    nsv5161433mobile element insertion1nstd203human GRCh38 chr22: 38,786,573-38,786,586 , GRCh37.p13 chr22: 39,182,578-39,182,591 DNAL4
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