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 200

    loading data ...

    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
    nsv7061751inversion1nstd229human GRCh38 chr16: 4,759,649-4,912,591 , GRCh37.p13 chr16: 4,809,650-4,962,592 PPL, ZNF500, 6 more genes
    nsv6977832copy number variation1nstd229human GRCh38 chr16: 4,773,566-4,777,928 , GRCh37.p13 chr16: 4,823,567-4,827,929 SEPTIN12
    nsv6976871copy number variation1nstd229human GRCh38 chr16: 4,698,229-4,805,227 , GRCh37.p13 chr16: 4,748,230-4,855,228 SMIM22, SEPTIN12, 5 more genes
    nsv6974259copy number variation1nstd229human GRCh38 chr16: 4,583,065-4,845,547 , GRCh37.p13 chr16: 4,633,066-4,895,548 DNAAF8, ANKS3, 12 more genes
    nsv6971341copy number variation1nstd229human GRCh38 chr16: 4,614,101-4,803,000 , GRCh37.p13 chr16: 4,664,102-4,853,001 MGRN1, ANKS3, 10 more genes
    nsv6969801copy number variation1nstd229human GRCh38 chr16: 4,771,962-4,780,180 , GRCh37.p13 chr16: 4,821,963-4,830,181 SEPTIN12
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 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
    nsv6623712copy number variation2nstd224human GRCh37 chr16: 4,828,087-4,838,323 , GRCh38.p12 chr16: 4,778,086-4,788,322 SEPTIN12, SMIM22
    nsv6623674copy number variation1nstd224human GRCh37 chr16: 4,810,583-4,829,726 , GRCh38.p12 chr16: 4,760,582-4,779,725 SEPTIN12, ZNF500
    nsv6594848inversion1nstd223human GRCh38 chr16: 4,759,650-4,912,583 , GRCh37.p13 chr16: 4,809,651-4,962,584 PPL, ZNF500, 6 more genes
    nsv6515410copy number variation1nstd223human GRCh38 chr16: 4,781,139-4,792,989 , GRCh37.p13 chr16: 4,831,140-4,842,990 SMIM22, SEPTIN12
    nsv6515275copy number variation1nstd223human GRCh38 chr16: 4,789,515-4,792,382 , GRCh37.p13 chr16: 4,839,516-4,842,383 SEPTIN12, SMIM22
    nsv6506010copy number variation1nstd223human GRCh38 chr16: 4,783,196-4,786,675 , GRCh37.p13 chr16: 4,833,197-4,836,676 SMIM22, SEPTIN12
    nsv6498421copy number variation1nstd223human GRCh38 chr16: 4,787,401-4,788,900 , GRCh37.p13 chr16: 4,837,402-4,838,901 SMIM22, SEPTIN12
    nsv6274388copy number variation1nstd214human GRCh38 chr16: 4,775,651-4,775,826 , GRCh37.p13 chr16: 4,825,652-4,825,827 SEPTIN12
    nsv6144367copy number variation1nstd206human GRCh38 chr16: 4,772,000-4,782,000 , GRCh37.p13 chr16: 4,822,001-4,832,001 SEPTIN12
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    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