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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3872220copy number variation1nstd102humanBenign GRCh37 chr1: 6,065,164-6,066,517 , GRCh38.p12 chr1: 6,005,104-6,006,457 KCNAB2
    nsv3885896copy number variation1nstd102humanBenign GRCh37 chr1: 6,065,164-6,065,532 , GRCh38.p12 chr1: 6,005,104-6,005,472 KCNAB2
    nsv3885552copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 6,051,187-6,158,763 , GRCh38.p12 chr1: 5,991,127-6,098,703 KCNAB2, NPHP4
    nsv4454243copy number variation1nstd102humanUncertain significance GRCh37 chr1: 6,103,234-6,230,157 , GRCh38.p12 chr1: 6,043,174-6,170,097 KCNAB2, CHD5
    nsv3886059copy number variation1nstd102humanUncertain significance GRCh37 chr1: 5,962,543-6,062,001 , GRCh38.p12 chr1: 5,902,483-6,001,941 KCNAB2, NPHP4
    nsv6310885copy number variation1nstd102humanUncertain significance GRCh37 chr1: 6,046,195-6,101,952 , GRCh38.p12 chr1: 5,986,135-6,041,892 KCNAB2, NPHP4
    nsv4451385copy number variation1nstd102humanUncertain significance GRCh37 chr1: 5,884,375-6,102,915 , GRCh38.p12 chr1: 5,824,315-6,042,855 KCNAB2, MIR4689, 1 more genes
    nsv3923716copy number variation1nstd102humanUncertain significance NCBI36 chr1: 5,809,839-6,016,181 , GRCh37.p13 chr1: 5,887,252-6,093,594 , GRCh38.p12 chr1: 5,827,192-6,033,534 KCNAB2, NPHP4, 1 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 KCNAB2, RPL9P11, 466 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 KCNAB2, 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 KCNAB2, MFFP1, 364 more genes
    nsv3873030copy number variation1nstd102humanPathogenic GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663 KCNAB2, 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 KCNAB2, PDPN, 333 more genes
    nsv3888433copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316 KCNAB2, AURKAIP1, 356 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 KCNAB2, 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 KCNAB2, PRKCZ-DT, 315 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 KCNAB2, VWA1, 311 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 KCNAB2, VAMP3, 245 more genes
    nsv4436631copy number variation1nstd102humanPathogenic GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784 KCNAB2, 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 KCNAB2, LOC105378593, 252 more genes
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