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Items: 1 to 20 of 316

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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
    nsv5520738copy number variation1nstd206human GRCh38 chr16: 88,714,667-88,714,725 , GRCh37.p13 chr16: 88,781,075-88,781,133 CTU2, PIEZO1, 1 more genes
    nsv5317031copy number variation1nstd204human GRCh37.p13 chr16: 88,779,471-88,787,641 , GRCh38.p13 chr16: 88,713,063-88,721,233 PIEZO1, CTU2, 1 more genes
    nsv5294769copy number variation1nstd204human GRCh38.p13 chr16: 88,713,351-88,721,204 , GRCh37.p13 chr16: 88,779,759-88,787,612 CTU2, MIR4722, 1 more genes
    nsv5289947copy number variation1nstd204human GRCh38.p13 chr16: 88,668,401-89,192,400 , GRCh37.p13 chr16: 88,734,809-89,258,808 , RNF166, 26 more genes
    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
    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
    nsv4630604copy number variation1nstd183human GRCh37 chr16: 88,770,621-88,909,788 , GRCh38.p12 chr16: 88,704,213-88,843,380 , MIR4722, 9 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
    nsv4623864copy number variation1nstd183human GRCh37 chr16: 88,773,738-88,818,586 , GRCh38.p12 chr16: 88,707,330-88,752,178 PIEZO1, CTU2, 3 more genes
    nsv4620682copy number variation1nstd183human GRCh37 chr16: 88,782,535-88,783,266 , GRCh38.p12 chr16: 88,716,127-88,716,858 MIR4722, PIEZO1
    nsv4457118copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,782,844-89,140,571 , GRCh38.p12 chr16: 88,716,436-89,074,163 LOC102724632, LOC107983950, 16 more genes
    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
    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
    nsv4427649copy number variation1nstd174human GRCh37 chr16: 88,750,161-88,993,580 , GRCh38.p12 chr16: 88,683,753-88,927,172 , CBFA2T3, 18 more genes
    nsv4386984copy number variation1nstd173human GRCh37 chr16: 88,782,845-88,909,838 , GRCh38.p12 chr16: 88,716,437-88,843,430 , GALNS, 7 more genes
    nsv4376535copy number variation1nstd173human GRCh37 chr16: 88,724,255-89,304,889 , GRCh38.p12 chr16: 88,657,847-89,238,481 , APRT, 29 more genes
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