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Items: 1 to 20 of 477

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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
    nsv7066398inversion1nstd229human GRCh38 chr16: 1,795,672-2,006,533 , GRCh37.p13 chr16: 1,845,673-2,056,534 LINC00254, HAGH, 18 more genes
    nsv7062980inversion1nstd229human GRCh38 chr16: 1,841,028-1,851,031 , GRCh37.p13 chr16: 1,891,029-1,901,032 MEIOB
    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
    nsv6976985copy number variation1nstd229human GRCh38 chr16: 1,845,548-1,850,584 , GRCh37.p13 chr16: 1,895,549-1,900,585 MEIOB
    nsv6976039copy number variation1nstd229human GRCh38 chr16: 1,830,186-1,900,449 , GRCh37.p13 chr16: 1,880,187-1,950,450 FAHD1, LINC02124, 2 more genes
    nsv6973366copy number variation1nstd229human GRCh38 chr16: 1,837,531-1,840,852 , GRCh37.p13 chr16: 1,887,532-1,890,853 MEIOB, FAHD1
    nsv6969594copy number variation1nstd229human GRCh38 chr16: 1,820,637-1,914,850 , GRCh37.p13 chr16: 1,870,638-1,964,851 MEIOB, HS3ST6, 4 more genes
    nsv6968586copy number variation1nstd229human GRCh38 chr16: 1,836,490-1,836,796 , GRCh37.p13 chr16: 1,886,491-1,886,797 FAHD1, MEIOB
    nsv6967251copy number variation1nstd229human GRCh38 chr16: 1,796,980-1,972,676 , GRCh37.p13 chr16: 1,846,981-2,022,677 TBL3, MEIOB, 14 more genes
    nsv6966682copy number variation1nstd229human GRCh38 chr16: 1,856,286-1,856,911 , GRCh37.p13 chr16: 1,906,287-1,906,912 MEIOB
    nsv6961258copy number variation1nstd229human GRCh38 chr16: 1,796,554-2,140,440 , GRCh37.p13 chr16: 1,846,555-2,190,441 NTHL1, MSRB1, 29 more genes
    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
    nsv6592966inversion1nstd223human GRCh38 chr16: 1,868,339-1,869,615 , GRCh37.p13 chr16: 1,918,340-1,919,616 MEIOB
    nsv6590780inversion1nstd223human GRCh38 chr16: 1,842,700-1,843,069 , GRCh37.p13 chr16: 1,892,701-1,893,070 MEIOB
    nsv6589714inversion1nstd223human GRCh38 chr16: 1,864,743-1,865,406 , GRCh37.p13 chr16: 1,914,744-1,915,407 MEIOB
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