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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5519942copy number variation1nstd206human GRCh38 chr16: 29,446,486-30,285,000 , GRCh37.p13 chr16: 29,457,807-30,296,321 , CA5AP1, 57 more genes
    nsv5278356copy number variation1nstd204human GRCh38.p13 chr16: 29,460,001-29,464,900 , GRCh37.p13 chr16: 29,471,322-29,476,221 LOC388242, SLX1B-SULT1A4, 1 more genes
    nsv5274695copy number variation1nstd204human GRCh38.p13 chr16: 29,457,501-29,466,200 , GRCh37.p13 chr16: 29,468,822-29,477,521 LOC388242, SLX1B, 2 more genes
    nsv5272751copy number variation1nstd204human GRCh38.p13 chr16: 29,464,701-29,469,200 , GRCh37.p13 chr16: 29,476,022-29,480,521 , LOC388242, 2 more genes
    nsv5269080copy number variation1nstd204human GRCh38.p13 chr16: 29,457,901-29,462,200 , GRCh37.p13 chr16: 29,469,222-29,473,521 SLX1B, SLX1B-SULT1A4, 1 more genes
    nsv5267814copy number variation1nstd204human GRCh37.p13 chr16: 29,462,522-29,477,521 , GRCh38.p13 chr16: 29,451,201-29,466,200 SLX1B, LOC388242, 4 more genes
    nsv5263500copy number variation1nstd204human GRCh38.p13 chr16: 29,455,501-29,461,800 , GRCh37.p13 chr16: 29,466,822-29,473,121 SLX1B-SULT1A4, SLX1B, 1 more genes
    nsv5060036copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,443,322-30,320,321 , GRCh38.p12 chr16: 29,432,001-30,309,000 CORO1A, PRRT2, 55 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
    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
    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
    nsv4729893copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,448,001-30,302,100 , GRCh38.p12 chr16: 29,436,680-30,290,779 CDIPTOSP, SULT1A3, 55 more genes
    nsv4729767copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,383,808-30,177,240 , GRCh38.p12 chr16: 29,372,487-30,165,919 LOC388242, KIF22, 46 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
    nsv4685672copy number variation1nstd102humanrisk factor GRCh37 chr16: 29,446,604-30,218,886 , GRCh38.p12 chr16: 29,435,283-30,207,565 BOLA2-SMG1P6, HIRIP3, 53 more genes
    nsv4675855copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,212-30,178,406 , GRCh38.p12 chr16: 29,420,891-30,167,085 SULT1A4, SMG1P2, 45 more genes
    nsv4674913copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,178,406 , GRCh38.p12 chr16: 28,455,409-30,167,085 ATP2A1, IL27, 82 more genes
    nsv4672775copy number variation1nstd186human GRCh37 chr16: 29,473,255-29,478,487 , GRCh38.p12 chr16: 29,461,934-29,467,166 LOC388242, SULT1A4, 1 more genes
    nsv4669860copy number variation2nstd186human GRCh37 chr16: 29,362,873-29,616,190 , GRCh38.p12 chr16: 29,351,552-29,604,869 , BOLA2-SMG1P6, 13 more genes
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