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Items: 1 to 20 of 167

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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
    nsv7067613inversion1nstd229human GRCh38 chr16: 4,190,116-4,246,649 , GRCh37.p13 chr16: 4,240,117-4,296,650 LINC01569, SRL
    nsv7066004inversion1nstd229human GRCh38 chr16: 4,190,914-4,253,701 , GRCh37.p13 chr16: 4,240,915-4,303,702 LINC01569, SRL
    nsv6977808copy number variation1nstd229human GRCh38 chr16: 4,252,966-4,256,790 , GRCh37.p13 chr16: 4,302,967-4,306,791 LINC01569, TFAP4
    nsv6977076copy number variation1nstd229human GRCh38 chr16: 4,212,270-4,606,613 , GRCh37.p13 chr16: 4,262,271-4,656,614 VASN, C16orf96, 13 more genes
    nsv6974249copy number variation1nstd229human GRCh38 chr16: 4,253,667-4,253,753 , GRCh37.p13 chr16: 4,303,668-4,303,754 LINC01569
    nsv6973733copy number variation1nstd229human GRCh38 chr16: 4,250,501-4,251,600 , GRCh37.p13 chr16: 4,300,502-4,301,601 LINC01569
    nsv6966041copy number variation1nstd229human GRCh38 chr16: 4,245,080-4,252,296 , GRCh37.p13 chr16: 4,295,081-4,302,297 LINC01569
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6509370copy number variation1nstd223human GRCh38 chr16: 4,250,524-4,251,566 , GRCh37.p13 chr16: 4,300,525-4,301,567 LINC01569
    nsv6314863copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,619,617-4,448,281 , GRCh37.p13 chr16: 3,669,618-4,498,282 TRAP1, CORO7-PAM16, 15 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6132990copy number variation1nstd213human GRCh37 chr16: 3,980,000-5,140,001 , GRCh38.p12 chr16: 3,929,999-5,090,000 ADCY9, HMOX2, 38 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
    nsv5927816copy number variation1nstd209human GRCh38 chr16: 4,253,667-4,253,751 , GRCh37.p13 chr16: 4,303,668-4,303,752 , LINC01569
    nsv5878195copy number variation1nstd209human GRCh38 chr16: 4,250,531-4,251,567 , GRCh37.p13 chr16: 4,300,532-4,301,568 LINC01569
    nsv5530801copy number variation1nstd206human GRCh38 chr16: 4,253,667-4,253,753 , GRCh37.p13 chr16: 4,303,668-4,303,754 , LINC01569
    nsv5518601copy number variation1nstd206human GRCh38 chr16: 4,250,208-4,251,566 , GRCh37.p13 chr16: 4,300,209-4,301,567 LINC01569
    nsv5380997copy number variation2nstd102humanUncertain significance GRCh37 chr16: 3,929,813-4,387,545 , GRCh38.p12 chr16: 3,879,812-4,337,544 DBIP3, ADCY9, 8 more genes
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