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Items: 1 to 20 of 285

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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
    nsv7073913inversion1nstd229human GRCh38 chr16: 1,683,909-1,796,668 , GRCh37.p13 chr16: 1,733,910-1,846,669 JPT2, SPSB3, 8 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
    nsv6977654copy number variation1nstd229human GRCh38 chr16: 1,592,232-1,728,113 , GRCh37.p13 chr16: 1,642,233-1,778,114 MAPK8IP3-AS1, JPT2, 4 more genes
    nsv6977037copy number variation1nstd229human GRCh38 chr16: 1,683,908-2,006,596 , GRCh37.p13 chr16: 1,733,909-2,056,597 RPS2, SNORA78, 28 more genes
    nsv6971367copy number variation1nstd229human GRCh38 chr16: 1,696,471-1,708,364 , GRCh37.p13 chr16: 1,746,472-1,758,365 JPT2, MAPK8IP3
    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
    nsv6964153copy number variation1nstd229human GRCh38 chr16: 1,677,110-1,678,823 , GRCh37.p13 chr16: 1,727,111-1,728,824 CRAMP1, JPT2
    nsv6960266copy number variation1nstd229human GRCh38 chr16: 1,675,563-1,678,811 , GRCh37.p13 chr16: 1,725,564-1,728,812 JPT2, CRAMP1
    nsv6959087copy number variation1nstd229human GRCh38 chr16: 1,654,605-1,688,965 , GRCh37.p13 chr16: 1,704,606-1,738,966 CRAMP1, JPT2
    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
    nsv6595307inversion1nstd223human GRCh38 chr16: 1,516,512-2,069,676 , GRCh37.p13 chr16: 1,566,513-2,119,677 MAPK8IP3-AS1, EME2, 37 more genes
    nsv6590598inversion1nstd223human GRCh38 chr16: 1,682,172-1,683,093 , GRCh37.p13 chr16: 1,732,173-1,733,094 JPT2
    nsv6514736copy number variation1nstd223human GRCh38 chr16: 1,679,835-1,684,509 , GRCh37.p13 chr16: 1,729,836-1,734,510 JPT2
    nsv6513584copy number variation1nstd223human GRCh38 chr16: 1,682,620-1,686,220 , GRCh37.p13 chr16: 1,732,621-1,736,221 JPT2
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