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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112663copy number variation1nstd102humanUncertain significance GRCh38 chr16: 28,812,342-29,035,950 , GRCh37.p13 chr16: 28,823,663-29,047,271 CD19, MIR4517, 12 more genes
    nsv5673078copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,827-28,950,294 , GRCh38.p12 chr16: 28,477,506-28,938,973 SH2B1, NUPR1, 21 more genes
    nsv5672755copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,668,059-29,001,338 , GRCh38.p12 chr16: 28,656,738-28,990,017 ATP2A1, CD19, 17 more genes
    nsv5527909copy number variation1nstd206human GRCh38 chr16: 28,840,787-28,840,908 , GRCh37.p13 chr16: 28,852,108-28,852,229 TUFM
    nsv5519512copy number variation1nstd206human GRCh38 chr16: 28,841,348-28,861,668 , GRCh37.p13 chr16: 28,852,669-28,872,989 MIR4721, SH2B1, 1 more genes
    nsv5278144copy number variation1nstd204human GRCh38.p13 chr16: 28,842,553-28,843,552 , GRCh37.p13 chr16: 28,853,874-28,854,873 TUFM, MIR4721
    nsv5266244copy number variation1nstd204human GRCh38.p13 chr16: 28,840,853-28,843,352 , GRCh37.p13 chr16: 28,852,174-28,854,673 MIR4721, TUFM
    nsv5264142copy number variation1nstd204human GRCh38.p13 chr16: 28,814,740-28,843,602 , GRCh37.p13 chr16: 28,826,061-28,854,923 TUFM, RPS15AP33, 2 more genes
    nsv5200383copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,615,644-29,042,118 , GRCh38.p12 chr16: 28,604,323-29,030,797 RPS15AP33, ATP2A1-AS1, 19 more genes
    nsv5003395copy number variation1nstd200human GRCh38 chr16: 28,840,936-28,847,844 , GRCh37.p13 chr16: 28,852,257-28,859,165 SH2B1, MIR4721, 1 more genes
    nsv4856748copy number variation1nstd200human GRCh37 chr16: 28,852,107-28,852,230 , GRCh38.p12 chr16: 28,840,786-28,840,909 TUFM
    nsv4769395copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,483,631-29,332,591 , GRCh38.p12 chr16: 28,472,310-29,321,270 MIR4517, SULT1A1, 33 more genes
    nsv4729970copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,819,028-28,988,225 , GRCh38.p12 chr16: 28,807,707-28,976,904 ATXN2L, NFATC2IP, 10 more genes
    nsv4729918copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,319-30,178,406 , GRCh38.p12 chr16: 28,476,998-30,167,085 SEZ6L2, C16orf92, 81 more genes
    nsv4729912copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,336,673-29,358,712 , GRCh38.p12 chr16: 28,325,352-29,347,391 ATP2A1-AS1, NPIPB8, 38 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729758copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,819,028-28,976,572 , GRCh38.p12 chr16: 28,807,707-28,965,251 MIR4517, SH2B1, 9 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
    nsv4685761copy number variation1nstd102humannot provided GRCh37 chr16: 21,312,200-29,646,379 , GRCh38.p12 chr16: 21,300,879-29,635,058 NUPR1, TNRC6A, 176 more genes
    nsv4684447copy number variation1nstd192human GRCh38.p12 chr16: 28,743,362-29,033,424 , GRCh37 chr16: 28,754,683-29,044,745 , ATP2A1, 14 more genes
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