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Items: 1 to 20 of 147

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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
    nsv6975475copy number variation1nstd229human GRCh38 chr16: 3,492,588-3,498,869 , GRCh37.p13 chr16: 3,542,588-3,548,869 C16orf90, RPL18P12
    nsv6972900copy number variation1nstd229human GRCh38 chr16: 3,490,428-3,498,527 , GRCh37.p13 chr16: 3,540,428-3,548,527 RPL18P12, C16orf90
    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
    nsv6965556copy number variation1nstd229human GRCh38 chr16: 3,492,601-3,498,800 , GRCh37.p13 chr16: 3,542,601-3,548,800 RPL18P12, C16orf90
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6514045copy number variation1nstd223human GRCh38 chr16: 3,489,101-3,498,500 , GRCh37.p13 chr16: 3,539,101-3,548,500 C16orf90, RPL18P12
    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
    nsv6144827copy number variation1nstd206human GRCh38 chr16: 3,491,792-3,503,249 , GRCh37.p13 chr16: 3,541,792-3,553,249 RPL18P12, C16orf90, 1 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
    nsv6034316copy number variation1nstd212human GRCh38 chr16: 3,492,033-3,503,452 , GRCh37.p13 chr16: 3,542,033-3,553,452 CLUAP1, RPL18P12, 1 more genes
    nsv5380855copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,543,839-3,551,089 , GRCh38.p12 chr16: 3,493,839-3,501,089 CLUAP1, RPL18P12, 1 more genes
    nsv5315443copy number variation1nstd204human GRCh38.p13 chr16: 3,474,896-3,519,212 , GRCh37.p13 chr16: 3,524,896-3,569,212 CLUAP1, MIR6126, 3 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
    nsv5264434copy number variation1nstd204human GRCh38.p13 chr16: 3,477,311-3,492,223 , GRCh37.p13 chr16: 3,527,311-3,542,223 MIR6126, NAA60, 1 more genes
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