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Items: 1 to 20 of 323

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138819insertion1nstd232human GRCh37.p13 chr1: 169,523,397-169,523,397 , GRCh38.p12 chr1: 169,554,159-169,554,159 F5
    nsv6644477copy number variation1nstd229human GRCh38 chr1: 169,578,657-169,844,806 , GRCh37.p13 chr1: 169,547,895-169,813,947 F5, SELE, 6 more genes
    nsv6644475copy number variation1nstd229human GRCh38 chr1: 169,566,040-169,566,433 , GRCh37.p13 chr1: 169,535,278-169,535,671 F5
    nsv6644474copy number variation1nstd229human GRCh38 chr1: 169,554,084-169,554,180 , GRCh37.p13 chr1: 169,523,322-169,523,418 F5
    nsv6644472copy number variation1nstd229human GRCh38 chr1: 169,541,501-169,546,700 , GRCh37.p13 chr1: 169,510,739-169,515,938 F5
    nsv6644404copy number variation1nstd229human GRCh38 chr1: 169,553,825-169,559,062 , GRCh37.p13 chr1: 169,523,063-169,528,300 F5
    nsv6644403copy number variation1nstd229human GRCh38 chr1: 169,521,501-169,639,600 , GRCh37.p13 chr1: 169,490,739-169,608,838 SELP, F5
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644034copy number variation1nstd229human GRCh38 chr1: 169,559,405-169,560,697 , GRCh37.p13 chr1: 169,528,643-169,529,935 F5
    nsv6625875copy number variation1nstd224human GRCh37 chr1: 169,547,458-170,642,899 , GRCh38.p12 chr1: 169,578,220-170,673,758 SELP, GORAB, 23 more genes
    nsv6325091copy number variation1nstd223human GRCh38 chr1: 169,553,824-169,559,060 , GRCh37.p13 chr1: 169,523,062-169,528,298 F5
    nsv6324641copy number variation1nstd223human GRCh38 chr1: 169,524,367-169,525,126 , GRCh37.p13 chr1: 169,493,605-169,494,364 F5
    nsv6323988copy number variation1nstd223human GRCh38 chr1: 169,538,686-169,539,407 , GRCh37.p13 chr1: 169,507,924-169,508,645 F5
    nsv6320202copy number variation1nstd223human GRCh38 chr1: 169,569,285-169,569,906 , GRCh37.p13 chr1: 169,538,523-169,539,144 F5
    nsv6319053copy number variation1nstd223human GRCh38 chr1: 169,561,301-169,564,200 , GRCh37.p13 chr1: 169,530,539-169,533,438 F5
    nsv6316754copy number variation1nstd223human GRCh38 chr1: 169,517,380-169,517,905 , GRCh37.p13 chr1: 169,486,618-169,487,143 F5
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6297455copy number variation1nstd186human GRCh37 chr1: 169,505,605-169,505,661 , GRCh38.p12 chr1: 169,536,367-169,536,423 F5
    nsv6214621insertion4nstd214human GRCh38 chr1: 169,554,159-169,554,159 , GRCh37.p13 chr1: 169,523,397-169,523,397 F5
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