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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3896638copy number variation1nstd102humanBenign GRCh37 chr11: 134,253,572-134,425,833 , GRCh38.p12 chr11: 134,383,678-134,555,939 B3GAT1, B3GAT1-DT
    nsv3876687copy number variation2nstd102humanBenign GRCh37 chr1: 145,625,979-145,901,548 , GRCh38.p12 chr1: 145,601,946-145,809,105 CD160, GPR89A, 3 more genes
    nsv3883047copy number variation1nstd102humanBenign GRCh37 chr1: 145,625,979-145,807,817 , GRCh38.p12 chr1: 145,627,236-145,809,105 PDZK1, RNF115, 2 more genes
    nsv3870684copy number variation2nstd102humanUncertain significance, Benign GRCh37 chr1: 145,626,237-145,735,326 , GRCh38.p12 chr1: 145,699,739-145,808,847 PDZK1, RNF115, 1 more genes
    nsv4676028copy number variation1nstd102humanLikely benign GRCh37 chr11: 134,163,400-134,378,532 , GRCh38.p12 chr11: 134,293,506-134,508,638 B3GAT1, B3GAT1-DT, 3 more genes
    nsv3899444copy number variation1nstd102humanBenign NCBI36 chr1: 144,331,465-144,646,997 , GRCh37 chr1: 145,620,108-145,935,640 , GRCh38 chr1: 145,601,946-145,814,985 RNF115, NBPF25P, 3 more genes
    nsv3908237copy number variation1nstd102humanBenign GRCh38 chr1: 145,603,343-145,808,847 , GRCh37 chr1: 145,626,237-145,831,720 , NCBI36 chr1: 144,337,594-144,543,077 PDZK1, CD160, 3 more genes
    nsv3881267copy number variation1nstd102humanBenign GRCh37 chr1: 145,598,991-145,747,925 , GRCh38.p12 chr1: 145,687,139-145,836,119 RNF115, POLR3C, 2 more genes
    nsv3877546copy number variation2nstd102humanBenign GRCh37 chr1: 145,625,979-145,762,959 , GRCh38.p12 chr1: 145,672,100-145,809,105 PDZK1, RNF115, 1 more genes
    nsv3888657copy number variation1nstd102humanBenign GRCh37 chr1: 145,611,279-145,735,326 , GRCh38.p12 chr1: 145,699,739-145,823,834 CD160, RNF115, 2 more genes
    nsv3890203copy number variation1nstd102humanBenign NCBI36 chr1: 144,331,465-144,446,683 , GRCh38 chr1: 145,699,739-145,814,985 , GRCh37 chr1: 145,620,108-145,735,326 CD160, RNF115, 1 more genes
    nsv3882626copy number variation1nstd102humanBenign GRCh37 chr1: 145,629,470-145,727,253 , GRCh38.p12 chr1: 145,707,813-145,805,612 CD160, RNF115, 1 more genes
    nsv3889357copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,617,348-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,817,744 NBPF25P, CD160, 3 more genes
    nsv6637126copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,617,349-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,817,743 RNF115, GPR89A, 3 more genes
    nsv6636370copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,622,531-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,812,561 GPR89A, PDZK1, 3 more genes
    nsv4674804copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,625,128-145,958,362 , GRCh38.p12 chr1: 145,601,946-145,809,957 GPR89A, RNF115, 3 more genes
    nsv3892227copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,625,128-145,888,926 , GRCh38 chr1: 145,601,946-145,809,957 , NCBI36 chr1: 144,336,485-144,600,283 NBPF25P, RNF115, 3 more genes
    nsv3873103copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,625,128-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,809,957 CD160, NBPF25P, 3 more genes
    nsv6290531copy number variation1nstd102humanUncertain significance GRCh37 chr1: 145,625,129-145,888,926 , GRCh38.p12 chr1: 145,601,946-145,809,956 GPR89A, RNF115, 3 more genes
    nsv3903287copy number variation2nstd102humanUncertain significance GRCh38 chr1: 145,601,946-145,807,381 , NCBI36 chr1: 144,339,058-144,655,669 , GRCh37 chr1: 145,627,701-145,944,312 CD160, GPR89A, 3 more genes
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