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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094579copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,712,146-31,021,717 , GRCh38.p12 chr16: 30,700,825-31,010,396 FBXL19-AS1, BCL7C, 19 more genes
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7062648inversion1nstd229human GRCh38 chr16: 30,991,645-30,995,683 , GRCh37.p13 chr16: 31,002,966-31,007,004 STX1B
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6992677copy number variation1nstd229human GRCh38 chr16: 30,859,398-31,135,376 , GRCh37.p13 chr16: 30,870,719-31,146,697 SETD1A, HSD3B7, 19 more genes
    nsv6990871copy number variation1nstd229human GRCh38 chr16: 30,902,101-31,224,500 , GRCh37.p13 chr16: 30,913,422-31,235,821 CTF2P, VKORC1, 22 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
    nsv6309670copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,996,980-31,021,717 , GRCh38.p12 chr16: 30,985,659-31,010,396 STX1B, HSD3B7
    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
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4786068mobile element deletion1nstd200human GRCh37 chr16: 31,006,810-31,007,111 , GRCh38.p12 chr16: 30,995,489-30,995,790 STX1B
    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
    nsv4729848copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,973,518-31,001,721 , GRCh38.p12 chr16: 30,962,197-30,990,400 STX1B, HSD3B7, 1 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
    nsv4550982insertion1nstd166human GRCh37.p13 chr16: 31,010,558-31,010,558 , GRCh38.p12 chr16: 30,999,237-30,999,237 STX1B
    nsv4455315copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,851,860-31,156,762 , GRCh38.p12 chr16: 30,840,539-31,145,441 LOC101928762, ZNF646, 20 more genes
    nsv4454134copy number variation1nstd102humanPathogenic GRCh37 chr16: 31,012,229-31,012,944 , GRCh38 chr16: 31,000,908-31,001,623 STX1B
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