U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 163

    loading data ...

    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
    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
    nsv6514113copy number variation1nstd223human GRCh38 chr16: 2,794,859-2,796,523 , GRCh37.p13 chr16: 2,844,860-2,846,524 PRSS41, SNORA3C
    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
    nsv6087658insertion1nstd212human GRCh38 chr16: 2,801,971-2,801,971 , GRCh37.p13 chr16: 2,851,972-2,851,972 PRSS41
    nsv6021694copy number variation1nstd212human GRCh38 chr16: 2,801,973-2,802,026 , GRCh37.p13 chr16: 2,851,974-2,852,027 PRSS41
    nsv5588676copy number variation1nstd207human GRCh38 chr16: 2,801,973-2,802,022 , GRCh37.p13 chr16: 2,851,974-2,852,023 PRSS41
    nsv5272285copy number variation1nstd204human GRCh38.p13 chr16: 2,651,201-3,235,500 , GRCh37.p13 chr16: 2,701,202-3,285,500 , RNU1-125P, 64 more genes
    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
    nsv5262390copy number variation1nstd204human GRCh38.p13 chr16: 2,578,401-2,889,000 , GRCh37.p13 chr16: 2,628,402-2,939,001 PRSS30P, ELOB, 18 more genes
    nsv4735089copy number variation1nstd199human GRCh37 chr16: 2,851,937-2,851,989 , GRCh38.p12 chr16: 2,801,936-2,801,988 PRSS41
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center