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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 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
    nsv6968778copy number variation1nstd229human GRCh38 chr16: 3,206,227-3,444,939 , GRCh37.p13 chr16: 3,256,227-3,494,939 MEFV, ZNF597, 18 more genes
    nsv6968645copy number variation1nstd229human GRCh38 chr16: 3,403,933-3,529,577 , GRCh37.p13 chr16: 3,453,933-3,579,577 CLUAP1, C16orf90, 5 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
    nsv6513433copy number variation1nstd223human GRCh38 chr16: 3,442,670-3,450,668 , GRCh37.p13 chr16: 3,492,670-3,500,668 ZNF597, NAA60
    nsv6508168copy number variation1nstd223human GRCh38 chr16: 3,418,478-3,445,377 , GRCh37.p13 chr16: 3,468,478-3,495,377 NAA60, ZNF597
    nsv6506064copy number variation1nstd223human GRCh38 chr16: 3,440,495-3,442,451 , GRCh37.p13 chr16: 3,490,495-3,492,451 NAA60, ZNF597
    nsv6501672copy number variation1nstd223human GRCh38 chr16: 3,442,661-3,450,686 , GRCh37.p13 chr16: 3,492,661-3,500,686 ZNF597, NAA60
    nsv6310074copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,293,141-3,929,917 , GRCh38.p12 chr16: 3,243,141-3,879,916 MTRNR2L4, TRAP1, 26 more genes
    nsv6290044copy number variation1nstd218human GRCh38.p12 chr16: 2,757,479-3,781,321 , GRCh37 chr16: 2,807,480-3,831,322 , CREBBP, 87 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133274copy number variation1nstd213human GRCh37 chr16: 2,660,000-3,710,001 , GRCh38.p12 chr16: 2,609,999-3,660,000 DNASE1, MEFV, 90 more genes
    nsv6133023copy number variation1nstd213human GRCh37 chr16: 3,410,000-3,550,001 , GRCh38.p12 chr16: 3,360,000-3,500,001 ZNF174, CLUAP1, 12 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5533533copy number variation1nstd206human GRCh38 chr16: 3,442,675-3,450,714 , GRCh37.p13 chr16: 3,492,675-3,500,714 NAA60, ZNF597
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5268408copy number variation1nstd204human GRCh37.p13 chr16: 3,468,501-3,580,000 , GRCh38.p13 chr16: 3,418,501-3,530,000 CLUAP1, NAA60, 4 more genes
    nsv4854352copy number variation1nstd200human GRCh37 chr16: 3,492,584-3,500,723 , GRCh38.p12 chr16: 3,442,584-3,450,723 NAA60, ZNF597
    nsv4854351copy number variation1nstd200human GRCh37 chr16: 3,470,363-3,490,572 , GRCh38.p12 chr16: 3,420,363-3,440,572 ZNF597
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