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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901898copy number variation1nstd102humanBenign GRCh37 chr16: 8,755,653-8,764,428 , GRCh38.p12 chr16: 8,661,796-8,670,571 METTL22
    nsv3902217copy number variation1nstd102humanBenign GRCh37 chr16: 8,722,052-8,875,529 , GRCh38.p12 chr16: 8,628,195-8,781,672 METTL22, RNU7-63P, 3 more genes
    nsv4729529copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,687,669-8,797,595 , GRCh38.p12 chr16: 8,593,818-8,703,738 METTL22, RN7SL743P, 2 more genes
    nsv4455392copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,635,993-8,788,833 , GRCh38.p12 chr16: 8,585,991-8,694,976 METTL22, ABAT, 2 more genes
    nsv4675091copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,741,774-8,798,255 , GRCh38.p12 chr16: 8,647,917-8,704,398 METTL22, ABAT, 2 more genes
    nsv4456350copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,727,589-8,874,779 , GRCh38.p12 chr16: 8,633,732-8,780,922 METTL22, RNU7-63P, 3 more genes
    nsv4455654copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,621,331-8,803,621 , GRCh38.p12 chr16: 8,571,329-8,709,764 METTL22, RN7SL743P, 3 more genes
    nsv3919049copy number variation1nstd102humanUncertain significance NCBI36 chr16: 8,599,283-8,729,853 , GRCh37.p13 chr16: 8,691,782-8,822,352 , GRCh38.p12 chr16: 8,597,925-8,728,495 METTL22, ABAT, 2 more genes
    nsv4455701copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,729,039-8,819,705 , GRCh38.p12 chr16: 8,635,182-8,725,848 METTL22, ABAT, 2 more genes
    nsv4457077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,766,187-8,822,840 , GRCh38.p12 chr16: 8,672,330-8,728,983 METTL22, RN7SL743P, 2 more genes
    nsv7098957copy number variation1nstd102humanPathogenic GRCh37 chr16: 8,160,554-9,074,348 , GRCh38.p12 chr16: 8,110,552-8,980,491 METTL22, ABAT, 14 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 METTL22, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 METTL22, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 METTL22, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 METTL22, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 METTL22, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 METTL22, LOC105371069, 654 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 METTL22, BMERB1, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 METTL22, NPIPB9, 597 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 METTL22, MIR6511B2, 535 more genes
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