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Items: 1 to 20 of 178

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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
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 CSF2RBP1, H1-0, 80 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 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
    nsv7067151inversion1nstd229human GRCh38 chr22: 37,862,494-37,904,603 , GRCh37.p13 chr22: 38,258,501-38,300,610 RNU6-900P, EIF3L, 1 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
    nsv7033927copy number variation1nstd229human GRCh38 chr22: 37,937,792-37,940,706 , GRCh37.p13 chr22: 38,333,799-38,336,713 MICALL1
    nsv7033825copy number variation1nstd229human GRCh38 chr22: 37,902,446-37,907,900 , GRCh37.p13 chr22: 38,298,453-38,303,907 MICALL1
    nsv7033533copy number variation1nstd229human GRCh38 chr22: 37,926,960-37,933,198 , GRCh37.p13 chr22: 38,322,967-38,329,205 MICALL1
    nsv7028315copy number variation1nstd229human GRCh38 chr22: 37,937,777-37,937,906 , GRCh37.p13 chr22: 38,333,784-38,333,913 MICALL1
    nsv7027806copy number variation1nstd229human GRCh38 chr22: 37,935,988-37,967,204 , GRCh37.p13 chr22: 38,331,995-38,363,211 MIR6820, MICALL1, 2 more genes
    nsv7026915copy number variation1nstd229human GRCh38 chr22: 37,904,165-37,911,779 , GRCh37.p13 chr22: 38,300,172-38,307,786 MICALL1
    nsv6543139copy number variation1nstd223human GRCh38 chr22: 37,934,943-37,936,095 , GRCh37.p13 chr22: 38,330,950-38,332,102 MICALL1
    nsv6541586copy number variation1nstd223human GRCh38 chr22: 37,904,165-37,911,779 , GRCh37.p13 chr22: 38,300,172-38,307,786 MICALL1
    nsv6537808copy number variation1nstd223human GRCh38 chr22: 37,933,415-37,948,986 , GRCh37.p13 chr22: 38,329,422-38,344,993 C22orf23, MICALL1
    nsv6537792copy number variation1nstd223human GRCh38 chr22: 37,902,446-37,907,895 , GRCh37.p13 chr22: 38,298,453-38,303,902 MICALL1
    nsv6313943copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 38,116,341-38,369,048 , GRCh38.p12 chr22: 37,720,334-37,973,041 H1-0, POLR2F, 13 more genes
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