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Items: 1 to 20 of 359

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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
    nsv7077985inversion1nstd229human GRCh38 chr16: 1,333,340-1,353,764 , GRCh37.p13 chr16: 1,383,341-1,403,765 GNPTG, BAIAP3, 1 more genes
    nsv7073654inversion1nstd229human GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907 UBE2I, CRAMP1, 45 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
    nsv6977134copy number variation1nstd229human GRCh38 chr16: 951,401-1,472,200 , GRCh37.p13 chr16: 1,001,401-1,522,201 TPSG1, TPSAB1, 27 more genes
    nsv6976551copy number variation1nstd229human GRCh38 chr16: 1,336,430-1,451,010 , GRCh37.p13 chr16: 1,386,431-1,501,011 LOC101929440, CCDC154, 9 more genes
    nsv6973759copy number variation1nstd229human GRCh38 chr16: 1,343,657-1,347,514 , GRCh37.p13 chr16: 1,393,658-1,397,515 BAIAP3, TSR3
    nsv6969363copy number variation1nstd229human GRCh38 chr16: 1,231,537-1,395,440 , GRCh37.p13 chr16: 1,281,538-1,445,441 PRSS29P, RPS20P2, 10 more genes
    nsv6968644copy number variation1nstd229human GRCh38 chr16: 1,319,632-1,358,036 , GRCh37.p13 chr16: 1,369,633-1,408,037 TSR3, UBE2I, 3 more genes
    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
    nsv6965059copy number variation1nstd229human GRCh38 chr16: 1,338,388-1,447,609 , GRCh37.p13 chr16: 1,388,389-1,497,610 GNPTG, UNKL, 9 more genes
    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
    nsv6958674copy number variation1nstd229human GRCh38 chr16: 1,348,858-1,349,575 , GRCh37.p13 chr16: 1,398,859-1,399,576 BAIAP3, TSR3
    nsv6637768copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054 CRAMP1, LOC105371046, 57 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
    nsv6623402copy number variation1nstd224human GRCh37 chr16: 1,371,154-1,421,606 , GRCh38.p12 chr16: 1,321,153-1,371,605 UBE2I, BAIAP3, 5 more genes
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