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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137713insertion1nstd232human GRCh37.p13 chr1: 6,618,974-6,618,974 , GRCh38.p12 chr1: 6,558,914-6,558,914 TAS1R1
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052066inversion1nstd229human GRCh38 chr1: 4,379,650-7,782,927 , GRCh37.p13 chr1: 4,439,710-7,842,987 NPHP4, MIR4252, 46 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv6653442copy number variation1nstd229human GRCh38 chr1: 6,576,901-6,580,100 , GRCh37.p13 chr1: 6,636,961-6,640,160 LOC107984912, TAS1R1, 1 more genes
    nsv6653435copy number variation1nstd229human GRCh38 chr1: 6,554,193-6,614,241 , GRCh37.p13 chr1: 6,614,253-6,674,301 KLHL21, NOL9, 5 more genes
    nsv6653200copy number variation1nstd229human GRCh38 chr1: 6,552,305-6,559,310 , GRCh37.p13 chr1: 6,612,365-6,619,370 NOL9, TAS1R1
    nsv6652673copy number variation1nstd229human GRCh38 chr1: 6,520,417-6,587,903 , GRCh37.p13 chr1: 6,580,477-6,647,963 LOC107984912, TAS1R1, 4 more genes
    nsv6652370copy number variation1nstd229human GRCh38 chr1: 6,261,636-6,608,517 , GRCh37.p13 chr1: 6,321,696-6,668,577 LOC107984913, ZBTB48, 11 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636950copy number variation1nstd102humanPathogenic GRCh37 chr1: 5,505,039-7,027,995 , GRCh38.p12 chr1: 5,444,979-6,967,935 RPL37P9, PHF13, 31 more genes
    nsv6549892inversion1nstd223human GRCh38 chr1: 6,558,912-6,559,723 , GRCh37.p13 chr1: 6,618,972-6,619,783 TAS1R1
    nsv6331289copy number variation1nstd223human GRCh38 chr1: 6,566,726-6,573,806 , GRCh37.p13 chr1: 6,626,786-6,633,866 TAS1R1, LOC107984912
    nsv6329098copy number variation1nstd223human GRCh38 chr1: 6,520,417-6,587,903 , GRCh37.p13 chr1: 6,580,477-6,647,963 PLEKHG5, NOL9, 4 more genes
    nsv6327894copy number variation1nstd223human GRCh38 chr1: 6,567,476-6,568,371 , GRCh37.p13 chr1: 6,627,536-6,628,431 TAS1R1, LOC107984912
    nsv6327122copy number variation1nstd223human GRCh38 chr1: 6,567,464-6,568,331 , GRCh37.p13 chr1: 6,627,524-6,628,391 TAS1R1, LOC107984912
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