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Items: 1 to 20 of 584

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7094663copy number variation2nstd102humanPathogenic GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266 TPSP2, PRR25, 83 more genes
    nsv6976635copy number variation1nstd229human GRCh38 chr16: 768,102-787,914 , GRCh37.p13 chr16: 818,102-837,914 CHTF18, MIR662, 3 more genes
    nsv6975349copy number variation1nstd229human GRCh38 chr16: 782,856-786,838 , GRCh37.p13 chr16: 832,856-836,838 RPUSD1, CHTF18
    nsv6973147copy number variation1nstd229human GRCh38 chr16: 769,739-790,316 , GRCh37.p13 chr16: 819,739-840,316 CHTF18, MIR662, 2 more genes
    nsv6971814copy number variation1nstd229human GRCh38 chr16: 774,869-792,888 , GRCh37.p13 chr16: 824,869-842,888 RPUSD1, MSLNL, 1 more genes
    nsv6637972copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185 MPG, LOC105371038, 78 more genes
    nsv6637644copy number variation1nstd102humanUncertain significance GRCh37 chr16: 726,789-1,066,511 , GRCh38.p12 chr16: 676,789-1,016,511 WDR24, STUB1, 21 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6623983copy number variation1nstd224human GRCh37 chr16: 818,452-883,851 , GRCh38.p12 chr16: 768,452-833,851 MSLN, GNG13, 5 more genes
    nsv6623932copy number variation1nstd224human GRCh37 chr16: 820,603-875,402 , GRCh38.p12 chr16: 770,603-825,402 GNG13, CHTF18, 4 more genes
    nsv6623931copy number variation1nstd224human GRCh37 chr16: 818,643-883,851 , GRCh38.p12 chr16: 768,643-833,851 MSLN, GNG13, 5 more genes
    nsv6623930copy number variation1nstd224human GRCh37 chr16: 818,523-875,402 , GRCh38.p12 chr16: 768,523-825,402 MSLN, GNG13, 5 more genes
    nsv6623782copy number variation1nstd224human GRCh37 chr16: 828,760-885,032 , GRCh38.p12 chr16: 778,760-835,032 RPUSD1, PRR25, 3 more genes
    nsv6623541copy number variation1nstd224human GRCh37 chr16: 818,802-878,324 , GRCh38.p12 chr16: 768,802-828,324 MSLN, GNG13, 5 more genes
    nsv6623540copy number variation1nstd224human GRCh37 chr16: 818,802-875,402 , GRCh38.p12 chr16: 768,802-825,402 MSLN, GNG13, 5 more genes
    nsv6623539copy number variation1nstd224human GRCh37 chr16: 818,452-878,324 , GRCh38.p12 chr16: 768,452-828,324 MSLN, GNG13, 5 more genes
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