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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971279inversion1nstd209human GRCh38 chr16: 21,590,269-22,770,846 , GRCh37.p13 chr16: 21,601,590-22,782,167 CDR2, UQCRC2, 31 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5666339inversion1nstd207human GRCh38 chr16: 21,502,503-22,432,381 , GRCh37.p13 chr16: 21,513,824-22,443,702 CDR2, UQCRC2, 30 more genes
    nsv5530479copy number variation1nstd206human GRCh38 chr16: 21,581,999-21,832,743 , GRCh37.p13 chr16: 21,593,320-21,844,064 OTOA, NPIPB4, 8 more genes
    nsv5280101copy number variation1nstd204human GRCh37.p13 chr16: 21,594,422-21,748,121 , GRCh38.p13 chr16: 21,583,101-21,736,800 IGSF6, METTL9, 4 more genes
    nsv5280089copy number variation1nstd204human GRCh38.p13 chr16: 21,652,068-21,653,467 , GRCh37.p13 chr16: 21,663,389-21,664,788 METTL9, IGSF6
    nsv5279508copy number variation1nstd204human GRCh38.p13 chr16: 21,625,795-21,663,495 , GRCh37.p13 chr16: 21,637,116-21,674,816 METTL9, RNU6-196P, 3 more genes
    nsv5276904copy number variation1nstd204human GRCh38.p13 chr16: 21,640,358-21,641,457 , GRCh37.p13 chr16: 21,651,679-21,652,778 IGSF6, RNU6-196P, 2 more genes
    nsv5274656copy number variation1nstd204human GRCh38.p13 chr16: 21,651,368-21,652,467 , GRCh37.p13 chr16: 21,662,689-21,663,788 IGSF6, METTL9
    nsv5266945copy number variation1nstd204human GRCh38.p13 chr16: 21,650,301-21,654,900 , GRCh37.p13 chr16: 21,661,622-21,666,221 IGSF6, METTL9
    nsv5266854copy number variation1nstd204human GRCh38.p13 chr16: 21,647,638-21,648,637 , GRCh37.p13 chr16: 21,658,959-21,659,958 IGSF6, METTL9
    nsv5263228copy number variation1nstd204human GRCh38.p13 chr16: 21,647,238-21,648,537 , GRCh37.p13 chr16: 21,658,559-21,659,858 IGSF6, METTL9
    nsv4994540copy number variation1nstd200human GRCh38 chr16: 21,641,914-21,643,359 , GRCh37.p13 chr16: 21,653,235-21,654,680 RNU6-196P, METTL9, 2 more genes
    nsv4864052copy number variation1nstd200human GRCh37 chr16: 21,653,235-21,654,680 , GRCh38.p12 chr16|NW_017852933.1: 1,461,469-1,462,914 , GRCh38.p12 chr16: 21,641,914-21,643,359 RNU6-1005P, IGSF6, 2 more genes
    nsv4756737inversion1nstd199human GRCh37 chr16: 21,594,441-22,710,750 , GRCh38.p12 chr16: 21,583,120-22,699,429 CDR2, UQCRC2, 31 more genes
    nsv4730273inversion26nstd198human GRCh38 chr16: 21,320,284-22,701,560 , GRCh37.p13 chr16: 21,331,605-22,712,881 CDR2, UQCRC2, 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
    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
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