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Items: 1 to 20 of 158

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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
    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
    nsv6964899copy number variation1nstd229human GRCh38 chr16: 4,258,947-4,259,483 , GRCh37.p13 chr16: 4,308,948-4,309,484 TFAP4
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    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
    nsv6023268copy number variation1nstd212human GRCh38 chr16: 4,258,957-4,259,033 , GRCh37.p13 chr16: 4,308,958-4,309,034 TFAP4
    nsv5532065copy number variation1nstd206human GRCh38 chr16: 4,258,985-4,259,535 , GRCh37.p13 chr16: 4,308,986-4,309,536 TFAP4
    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
    nsv5149498mobile element insertion1nstd203human GRCh38 chr16: 4,256,643-4,256,648 , GRCh37.p13 chr16: 4,306,644-4,306,649 TFAP4
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4683689copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,777,699-4,852,592 , GRCh38.p12 chr16: 3,727,698-4,802,591 UBALD1, HMOX2, 30 more genes
    nsv4683275copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,794,875-4,387,545 , GRCh38.p12 chr16: 3,744,874-4,337,544 GLIS2-AS1, LOC105371062, 8 more genes
    nsv4675826copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,651,354-4,614,965 , GRCh38.p12 chr16: 2,601,353-4,564,964 MEFV, TRR-CCT5-1, 111 more genes
    nsv4456586copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,469,027-4,328,143 , GRCh38.p12 chr16: 3,419,027-4,278,142 RPL18P12, ADCY9, 18 more genes
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