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Items: 1 to 20 of 68

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880921copy number variation1nstd102humanBenign GRCh37 chr1: 6,523,430-6,560,363 , GRCh38.p12 chr1: 6,463,370-6,500,303 TNFRSF25, PLEKHG5
    nsv3887378copy number variation1nstd102humanBenign GRCh37 chr1: 6,523,430-6,534,600 , GRCh38.p12 chr1: 6,463,370-6,474,540 TNFRSF25, PLEKHG5
    nsv3888528copy number variation1nstd102humanBenign GRCh37 chr1: 6,523,430-6,534,226 , GRCh38.p12 chr1: 6,463,370-6,474,166 TNFRSF25, PLEKHG5
    nsv3886937copy number variation1nstd102humanBenign GRCh37 chr1: 6,501,100-6,568,387 , GRCh38.p12 chr1: 6,441,040-6,508,327 TNFRSF25, ESPN, 1 more genes
    nsv3888806copy number variation1nstd102humanBenign GRCh37 chr1: 6,456,472-6,560,363 , GRCh38.p12 chr1: 6,396,412-6,500,303 TNFRSF25, HES2, 3 more genes
    nsv3885129copy number variation1nstd102humanBenign GRCh37 chr1: 6,440,288-6,520,312 , GRCh38.p12 chr1: 6,380,228-6,460,252 TNFRSF25, ESPN, 3 more genes
    nsv3885689copy number variation1nstd102humanBenign GRCh37 chr1: 6,481,916-6,560,363 , GRCh38.p12 chr1: 6,421,856-6,500,303 TNFRSF25, PLEKHG5, 2 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 TNFRSF25, RPL9P11, 466 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 TNFRSF25, LOC107985467, 386 more genes
    nsv3900501copy number variation1nstd102humanPathogenic GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016 TNFRSF25, MFFP1, 364 more genes
    nsv3873030copy number variation1nstd102humanPathogenic GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663 TNFRSF25, RN7SL451P, 376 more genes
    nsv3900236copy number variation1nstd102humanPathogenic GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383 TNFRSF25, PDPN, 333 more genes
    nsv3888433copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316 TNFRSF25, AURKAIP1, 356 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 TNFRSF25, 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 TNFRSF25, PRKCZ-DT, 315 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 TNFRSF25, VWA1, 311 more genes
    nsv3905483copy number variation1nstd102humanPathogenic GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588 TNFRSF25, VPS13D, 240 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 TNFRSF25, VAMP3, 245 more genes
    nsv4436631copy number variation1nstd102humanPathogenic GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784 TNFRSF25, LINC02606, 253 more genes
    nsv3913374copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327 TNFRSF25, LOC105378593, 252 more genes
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