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Items: 1 to 20 of 402

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137062copy number variation1nstd102humanUncertain significance GRCh37 chr22: 38,154,016-38,154,017 , GRCh38 chr22: 37,758,009-37,758,010 TRIOBP
    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
    nsv7095943copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,111,750-38,111,961 , GRCh38.p12 chr22: 37,715,743-37,715,954 TRIOBP
    nsv7095838copy number variation1nstd102humanUncertain significance GRCh37 chr22: 38,097,373-38,168,769 , GRCh38.p12 chr22: 37,701,366-37,772,762 LOC102724378, TRIOBP
    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
    nsv7093143copy number variation1nstd102humanUncertain significance GRCh38 chr22: 37,724,267-37,724,335 , GRCh37 chr22: 38,120,274-38,120,342 TRIOBP
    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
    nsv7072167inversion1nstd229human GRCh38 chr22: 37,711,032-37,726,972 , GRCh37.p13 chr22: 38,107,039-38,122,979 TRIOBP
    nsv7067150inversion1nstd229human GRCh38 chr22: 37,646,051-37,722,756 , GRCh37.p13 chr22: 38,042,058-38,118,763 LGALS1, NOL12, 5 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
    nsv7037270copy number variation1nstd229human GRCh38 chr22: 37,728,520-37,728,568 , GRCh37.p13 chr22: 38,124,527-38,124,575 TRIOBP
    nsv7037017copy number variation1nstd229human GRCh38 chr22: 37,724,801-37,758,300 , GRCh37.p13 chr22: 38,120,808-38,154,307 LOC102724378, TRIOBP
    nsv7035153copy number variation1nstd229human GRCh38 chr22: 37,668,255-37,711,471 , GRCh37.p13 chr22: 38,064,262-38,107,478 LGALS1, RN7SL385P, 2 more genes
    nsv7031802copy number variation1nstd229human GRCh38 chr22: 37,758,009-37,758,063 , GRCh37.p13 chr22: 38,154,016-38,154,070 TRIOBP
    nsv7031171copy number variation1nstd229human GRCh38 chr22: 37,716,380-37,719,112 , GRCh37.p13 chr22: 38,112,387-38,115,119 TRIOBP
    nsv7030702copy number variation1nstd229human GRCh38 chr22: 37,747,782-37,751,403 , GRCh37.p13 chr22: 38,143,789-38,147,410 TRIOBP
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