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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6987873copy number variation1nstd229human GRCh38 chr16: 30,594,684-30,601,809 , GRCh37.p13 chr16: 30,606,005-30,613,130 ZNF689
    nsv6984866copy number variation1nstd229human GRCh38 chr16: 30,610,122-30,610,370 , GRCh37.p13 chr16: 30,621,443-30,621,691 ZNF689
    nsv6637207copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,460,206-30,906,733 , GRCh38.p12 chr16: 30,448,885-30,895,412 ZNF629, ZNF689, 27 more genes
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6510051copy number variation1nstd223human GRCh38 chr16: 30,582,007-30,634,131 , GRCh37.p13 chr16: 30,593,328-30,645,452 ZNF689, ZNF785
    nsv6290347copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,808,153-30,750,270 , GRCh38.p12 chr16: 29,796,832-30,738,949 SULT1A3, SEPHS2, 65 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133022copy number variation1nstd213human GRCh37 chr16: 30,300,000-32,030,001 , GRCh38.p12 chr16: 30,288,679-32,018,680 COX6A2, CTF1, 91 more genes
    nsv5273947copy number variation1nstd204human GRCh38.p13 chr16: 30,595,079-30,601,077 , GRCh37.p13 chr16: 30,606,400-30,612,398 ZNF689
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv5003490copy number variation1nstd200human GRCh38 chr16: 30,596,986-30,600,690 , GRCh37.p13 chr16: 30,608,307-30,612,011 ZNF689
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv3924250copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,828,435-31,357,519 , GRCh37 chr16: 29,920,934-31,450,018 , GRCh38 chr16: 29,909,613-31,438,697 MIR4518, ZNF747-DT, 95 more genes
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