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Items: 1 to 20 of 31

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1007762copy number variation1nstd100human NCBI36 (hg18) chr2: 242,692,060-242,738,117 , GRCh37.p13 chr2|NW_003571031.1: 1-29,785 , GRCh38 (hg38) chr2: 242,101,236-242,147,293 0
    nsv1005488copy number variation3nstd100human NCBI36 (hg18) chr2: 242,682,948-242,738,117 , GRCh37.p13 chr2|NW_003571031.1: 1-29,785 , GRCh38 (hg38) chr2: 242,092,124-242,147,293 0
    nsv997369copy number variation4nstd100human GRCh38 (hg38) chr2: 242,095,106-242,147,293 , NCBI36 (hg18) chr2: 242,685,930-242,738,117 , GRCh37.p13 chr2|NW_003571031.1: 1-29,785 0
    nsv997342copy number variation1nstd100human GRCh38 (hg38) chr2: 242,090,159-242,147,293 , NCBI36 (hg18) chr2: 242,680,983-242,738,117 , GRCh37.p13 chr2|NW_003571031.1: 1-29,785 0
    esv3435911copy number variation1estd59human NCBI36 (hg18) chr16: 88,816,252-88,823,050 , GRCh37 (hg19) chr16: 90,288,751-90,295,549 , GRCh37.p13 chr2|NW_003571031.1: 49,636-56,427 , GRCh38 (hg38) chr16: 90,222,343-90,229,141 0
    esv3421431copy number variation1estd59human NCBI36 (hg18) chr16: 88,816,452-88,822,950 , GRCh37 (hg19) chr16: 90,288,951-90,295,449 , GRCh37.p13 chr2|NW_003571031.1: 49,836-56,327 , GRCh38 (hg38) chr16: 90,222,543-90,229,041 0
    esv3415231copy number variation1estd59human NCBI36 (hg18) chr2: 242,738,452-242,752,150 , GRCh37.p13 chr2|NW_003571031.1: 30,120-40,797 , GRCh37 (hg19) chr2: 243,089,779-243,100,456 , GRCh38 (hg38) chr2: 242,147,628-242,158,305 0
    esv3404386copy number variation1estd59human NCBI36 (hg18) chr16: 88,816,652-88,823,150 , GRCh37 (hg19) chr16: 90,289,151-90,295,649 , GRCh37.p13 chr2|NW_003571031.1: 50,036-56,527 , GRCh38 (hg38) chr16: 90,222,743-90,229,241 0
    esv3384865copy number variation1estd59human NCBI36 (hg18) chr2: 242,738,452-242,752,150 , GRCh37.p13 chr2|NW_003571031.1: 30,120-40,797 , GRCh37 (hg19) chr2: 243,089,779-243,100,456 , GRCh38 (hg38) chr2: 242,147,628-242,158,305 0
    esv3388850copy number variation1estd59human NCBI36 (hg18) chr2: 242,738,452-242,752,150 , GRCh37.p13 chr2|NW_003571031.1: 30,120-40,797 , GRCh37 (hg19) chr2: 243,089,779-243,100,456 , GRCh38 (hg38) chr2: 242,147,628-242,158,305 0
    esv3360798copy number variation1estd59human NCBI36 (hg18) chr2: 242,738,452-242,752,150 , GRCh37 (hg19) chr2: 243,089,779-243,100,456 , GRCh38 (hg38) chr2: 242,147,628-242,158,305 , GRCh37.p13 chr2|NW_003571031.1: 30,120-40,797 0
    esv3336971copy number variation1estd59human NCBI36 (hg18) chr16: 88,816,952-88,823,250 , GRCh37 (hg19) chr16: 90,289,451-90,295,749 , GRCh37.p13 chr2|NW_003571031.1: 50,336-56,627 , GRCh38 (hg38) chr16: 90,223,043-90,229,341 0
    esv3334054copy number variation1estd59human NCBI36 (hg18) chr2: 242,738,452-242,752,150 , GRCh37.p13 chr2|NW_003571031.1: 30,120-40,797 , GRCh37 (hg19) chr2: 243,089,779-243,100,456 , GRCh38 (hg38) chr2: 242,147,628-242,158,305 0
    esv3336063copy number variation1estd59human NCBI36 (hg18) chr2: 242,738,452-242,752,150 , GRCh37.p13 chr2|NW_003571031.1: 30,120-40,797 , GRCh37 (hg19) chr2: 243,089,779-243,100,456 , GRCh38 (hg38) chr2: 242,147,628-242,158,305 0
    nsv979282copy number variation48nstd82human NCBI36 (hg18) chr2: 242,743,886-242,747,177 , GRCh37.p13 chr2|NW_003571031.1: 35,554-38,845 , GRCh38 (hg38) chr2: 242,153,062-242,156,353 0
    nsv979193copy number variation80nstd82western gorilla NCBI36 (hg18) chr2: 242,717,262-242,751,255 , GRCh37.p13 chr2|NW_003571031.1: 8,930-39,797 , GRCh38 (hg38) chr2: 242,126,438-242,157,305 0
    nsv963867copy number variation1nstd82human NCBI36 (hg18) chr2: 242,739,923-242,743,886 , GRCh37.p13 chr2|NW_003571031.1: 31,591-35,554 , GRCh38 (hg38) chr2: 242,149,099-242,153,062 0
    nsv963866copy number variation1nstd82human NCBI36 (hg18) chr2: 242,727,532-242,733,177 , GRCh37.p13 chr2|NW_003571031.1: 19,200-24,845 , GRCh38 (hg38) chr2: 242,136,708-242,142,353 0
    nsv963865copy number variation80nstd82human NCBI36 (hg18) chr2: 242,715,019-242,717,262 , GRCh37.p13 chr2|NW_003571031.1: 6,687-8,930 , GRCh38 (hg38) chr2: 242,124,195-242,126,438 0
    nsv962027copy number variation48nstd82human NCBI36 (hg18) chr2: 242,727,532-242,743,886 , GRCh37.p13 chr2|NW_003571031.1: 19,200-35,554 , GRCh38 (hg38) chr2: 242,136,708-242,153,062 0
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