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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673007copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,709,737-89,220,635 , GRCh38.p12 chr16: 88,643,329-89,154,227 MIR4722, PIEZO1, 23 more genes
    nsv5514640copy number variation1nstd206human GRCh38 chr16: 88,641,302-88,654,895 , GRCh37.p13 chr16: 88,707,710-88,721,303 CYBA, MVD
    nsv5374749translocation1nstd200human GRCh38 chr16: 88,654,077-88,654,077 , GRCh38 chr16: 88,651,258-88,651,258 , GRCh37.p13 chr16: 88,717,666-88,717,666 , GRCh37.p13 chr16: 88,720,485-88,720,485 MVD, CYBA
    nsv5337566translocation1nstd200human GRCh37 chr16: 88,720,485-88,720,485 , GRCh37 chr16: 88,717,666-88,717,666 , GRCh38.p12 chr16: 88,651,258-88,651,258 , GRCh38.p12 chr16: 88,654,077-88,654,077 CYBA, MVD
    nsv5313509copy number variation1nstd204human GRCh38.p13 chr16: 88,652,749-88,654,254 , GRCh37.p13 chr16: 88,719,157-88,720,662 MVD
    nsv5290836copy number variation1nstd204human GRCh38.p13 chr16: 88,652,787-88,654,486 , GRCh37.p13 chr16: 88,719,195-88,720,894 MVD
    nsv5287779copy number variation1nstd204human GRCh38.p13 chr16: 88,301,301-89,068,700 , GRCh37.p13 chr16: 88,334,907-89,135,108 , ZFPM1-AS1, 33 more genes
    nsv5149837mobile element insertion1nstd203human GRCh38 chr16: 88,662,407-88,662,421 , GRCh37.p13 chr16: 88,728,815-88,728,829 MVD, SNAI3-AS1
    nsv5015041copy number variation1nstd200human GRCh38 chr16: 88,652,759-88,654,245 , GRCh37.p13 chr16: 88,719,167-88,720,653 MVD
    nsv4851010copy number variation1nstd200human GRCh37 chr16: 88,719,167-88,720,653 , GRCh38.p12 chr16: 88,652,759-88,654,245 MVD
    nsv4744784copy number variation1nstd199human GRCh37 chr16: 88,720,504-88,720,586 , GRCh38.p12 chr16: 88,654,096-88,654,178 MVD
    nsv4729945copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,222,732-90,155,062 , GRCh38.p12 chr16: 88,189,126-90,088,654 SNORD68, LOC105371412, 75 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4626010copy number variation2nstd183human GRCh37 chr16: 88,705,417-88,830,206 , GRCh38.p12 chr16: 88,639,009-88,763,798 PIEZO1, MIR4722, 9 more genes
    nsv4512991mobile element insertion1nstd166human GRCh37.p13 chr16: 88,728,815-88,728,815 , GRCh38.p12 chr16: 88,662,407-88,662,407 MVD, SNAI3-AS1
    nsv4456065copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,453,448-89,569,215 , GRCh38.p12 chr16: 88,387,040-89,502,807 LOC101927863, LINC00304, 45 more genes
    nsv4455948copy number variation1nstd102humanUncertain significance GRCh37 chr16: 87,848,902-88,809,407 , GRCh38.p12 chr16: 87,815,296-88,742,999 CYBA, BANP, 27 more genes
    nsv4455904copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,697,092-88,791,148 , GRCh38.p12 chr16: 88,630,684-88,724,740 ZC3H18, SNAI3, 8 more genes
    nsv4451072copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,709,737-88,718,353 , GRCh38 chr16: 88,643,329-88,651,945 MVD, CYBA
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
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