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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7059859inversion1nstd229human GRCh38 chr16: 2,780,687-2,815,616 , GRCh37.p13 chr16: 2,830,688-2,865,617 PRSS21, PRSS33, 2 more genes
    nsv6970961copy number variation1nstd229human GRCh38 chr16: 2,780,320-2,787,205 , GRCh37.p13 chr16: 2,830,321-2,837,206 PRSS33
    nsv6964379copy number variation1nstd229human GRCh38 chr16: 2,778,401-2,792,900 , GRCh37.p13 chr16: 2,828,402-2,842,901 PRSS33
    nsv6964031copy number variation1nstd229human GRCh38 chr16: 2,774,248-2,835,989 , GRCh37.p13 chr16: 2,824,249-2,885,990 PRSS41, ZG16B, 5 more genes
    nsv6962282copy number variation1nstd229human GRCh38 chr16: 2,780,325-2,806,305 , GRCh37.p13 chr16: 2,830,326-2,856,306 SNORA3C, PRSS33, 1 more genes
    nsv6637409copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,794,763-2,993,610 , GRCh38.p12 chr16: 2,744,762-2,943,609 RPL23AP86, FLYWCH1, 14 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
    nsv6512720copy number variation1nstd223human GRCh38 chr16: 2,778,366-2,792,889 , GRCh37.p13 chr16: 2,828,367-2,842,890 PRSS33
    nsv6507511copy number variation1nstd223human GRCh38 chr16: 2,780,325-2,806,304 , GRCh37.p13 chr16: 2,830,326-2,856,305 PRSS41, PRSS33, 1 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
    nsv6133194copy number variation1nstd213human GRCh37 chr16: 2,800,000-2,970,001 , GRCh38.p12 chr16: 2,749,999-2,920,000 ELOB, PRSS21, 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
    nsv6097948insertion1nstd212human GRCh38 chr16: 2,787,072-2,787,072 , GRCh37.p13 chr16: 2,837,073-2,837,073 PRSS33
    nsv6095903insertion1nstd212human GRCh38 chr16: 2,787,293-2,787,293 , GRCh37.p13 chr16: 2,837,294-2,837,294 PRSS33
    nsv6039669copy number variation1nstd212human GRCh38 chr16: 2,786,675-2,787,459 , GRCh37.p13 chr16: 2,836,676-2,837,460 PRSS33
    nsv6037880copy number variation1nstd212human GRCh38 chr16: 2,787,164-2,787,242 , GRCh37.p13 chr16: 2,837,165-2,837,243 PRSS33
    nsv5939667copy number variation1nstd209human GRCh38 chr16: 2,786,675-2,787,457 , GRCh37.p13 chr16: 2,836,676-2,837,458 PRSS33
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