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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673176copy number variation1nstd102humanPathogenic GRCh37 chr1: 954,503-992,499 , GRCh38.p12 chr1: 1,019,123-1,057,119 AGRN
    nsv3873975copy number variation1nstd102humanBenign GRCh37 chr1: 963,864-986,737 , GRCh38.p12 chr1: 1,028,484-1,051,357 AGRN
    nsv3885691copy number variation1nstd102humanBenign GRCh37 chr1: 963,938-985,900 , GRCh38.p12 chr1: 1,028,558-1,050,520 AGRN
    nsv3885196copy number variation1nstd102humanBenign GRCh37 chr1: 957,640-964,438 , GRCh38.p12 chr1: 1,022,260-1,029,058 AGRN
    nsv3874742copy number variation1nstd102humanBenign GRCh37 chr1: 963,864-964,438 , GRCh38.p12 chr1: 1,028,484-1,029,058 AGRN
    nsv3887240copy number variation1nstd102humanBenign GRCh37 chr1: 963,938-964,438 , GRCh38.p12 chr1: 1,028,558-1,029,058 AGRN
    nsv4683785copy number variation1nstd102humanUncertain significance GRCh37 chr1: 955,543-990,371 , GRCh38.p12 chr1: 1,020,163-1,054,991 AGRN
    nsv4682430copy number variation1nstd102humanUncertain significance GRCh37 chr1: 982,697-990,371 , GRCh38.p12 chr1: 1,047,317-1,054,991 AGRN
    nsv6311073copy number variation1nstd102humanUncertain significance GRCh37 chr1: 984,596-990,361 , GRCh38.p12 chr1: 1,049,216-1,054,981 AGRN
    nsv7096011copy number variation1nstd102humanUncertain significance GRCh37 chr1: 955,553-957,862 , GRCh38.p12 chr1: 1,020,173-1,022,482 AGRN
    nsv7093565insertion1nstd102humanUncertain significance GRCh38 chr1: 1,049,050-1,049,050 , GRCh37 chr1: 984,430-984,430 AGRN
    nsv3904205copy number variation2nstd102humanBenign/Likely benign, Benign GRCh38 chr1: 1,029,317-1,072,906 , GRCh37 chr1: 964,697-1,008,286 AGRN, LOC100288175, 2 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 AGRN, RPL9P11, 466 more genes
    nsv3873030copy number variation1nstd102humanPathogenic GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663 AGRN, RN7SL451P, 376 more genes
    nsv3888433copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316 AGRN, AURKAIP1, 356 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 AGRN, PARK7, 325 more genes
    nsv3899046copy number variation1nstd102humanPathogenic GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775 AGRN, PRKCZ-DT, 315 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 AGRN, VWA1, 311 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 AGRN, VAMP3, 245 more genes
    nsv4436631copy number variation1nstd102humanPathogenic GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784 AGRN, LINC02606, 253 more genes
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