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Items: 1 to 20 of 370

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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
    nsv7094812copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,550,077-1,553,023 , GRCh38.p12 chr16: 1,500,076-1,503,022 TELO2
    nsv7094811copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,496,632-1,561,171 , GRCh38.p12 chr16: 1,446,631-1,511,170 IFT140, CLCN7, 3 more genes
    nsv7094755copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,544,283-1,547,529 , GRCh38.p12 chr16: 1,494,282-1,497,528 TELO2
    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
    nsv7094557copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,555,391-1,555,622 , GRCh38.p12 chr16: 1,505,390-1,505,621 TELO2
    nsv7073654inversion1nstd229human GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907 UBE2I, CRAMP1, 45 more genes
    nsv7065492inversion1nstd229human GRCh38 chr16: 1,465,870-1,519,078 , GRCh37.p13 chr16: 1,515,871-1,569,079 RPS3AP2, IFT140, 3 more genes
    nsv7064563inversion1nstd229human GRCh38 chr16: 1,279,128-1,693,078 , GRCh37.p13 chr16: 1,329,129-1,743,079 UNKL, CRAMP1, 20 more genes
    nsv6976208copy number variation1nstd229human GRCh38 chr16: 1,498,834-1,501,401 , GRCh37.p13 chr16: 1,548,835-1,551,402 TELO2
    nsv6968802copy number variation1nstd229human GRCh38 chr16: 1,476,685-1,502,789 , GRCh37.p13 chr16: 1,526,686-1,552,790 RPS3AP2, PTX4, 1 more genes
    nsv6968191copy number variation1nstd229human GRCh38 chr16: 1,494,311-1,503,072 , GRCh37.p13 chr16: 1,544,312-1,553,073 TELO2
    nsv6967805copy number variation1nstd229human GRCh38 chr16: 1,493,515-1,495,665 , GRCh37.p13 chr16: 1,543,516-1,545,666 TELO2
    nsv6966737copy number variation1nstd229human GRCh38 chr16: 1,484,722-1,493,949 , GRCh37.p13 chr16: 1,534,723-1,543,950 TELO2, PTX4
    nsv6965261copy number variation1nstd229human GRCh38 chr16: 1,351,958-1,810,245 , GRCh37.p13 chr16: 1,401,959-1,860,246 JPT2, UNKL, 26 more genes
    nsv6964208copy number variation1nstd229human GRCh38 chr16: 1,510,646-1,513,954 , GRCh37.p13 chr16: 1,560,647-1,563,955 IFT140, TELO2
    nsv6962303copy number variation1nstd229human GRCh38 chr16: 1,118,142-1,673,202 , GRCh37.p13 chr16: 1,168,142-1,723,203 TJP1P1, TELO2, 27 more genes
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