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 369

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 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
    nsv7066398inversion1nstd229human GRCh38 chr16: 1,795,672-2,006,533 , GRCh37.p13 chr16: 1,845,673-2,056,534 LINC00254, HAGH, 18 more genes
    nsv6977037copy number variation1nstd229human GRCh38 chr16: 1,683,908-2,006,596 , GRCh37.p13 chr16: 1,733,909-2,056,597 RPS2, SNORA78, 28 more genes
    nsv6971016copy number variation1nstd229human GRCh38 chr16: 1,949,201-2,138,200 , GRCh37.p13 chr16: 1,999,202-2,188,201 MIR4516, NTHL1, 22 more genes
    nsv6967251copy number variation1nstd229human GRCh38 chr16: 1,796,980-1,972,676 , GRCh37.p13 chr16: 1,846,981-2,022,677 TBL3, MEIOB, 14 more genes
    nsv6964973copy number variation1nstd229human GRCh38 chr16: 1,980,449-1,982,329 , GRCh37.p13 chr16: 2,030,450-2,032,330 NOXO1, GFER, 1 more genes
    nsv6964603copy number variation1nstd229human GRCh38 chr16: 1,968,322-1,974,336 , GRCh37.p13 chr16: 2,018,323-2,024,337 TBL3, RNF151
    nsv6963890copy number variation1nstd229human GRCh38 chr16: 1,971,987-1,972,385 , GRCh37.p13 chr16: 2,021,988-2,022,386 TBL3
    nsv6962221copy number variation1nstd229human GRCh38 chr16: 1,948,840-1,970,124 , GRCh37.p13 chr16: 1,998,841-2,020,125 RPL3L, SNORA64, 7 more genes
    nsv6961258copy number variation1nstd229human GRCh38 chr16: 1,796,554-2,140,440 , GRCh37.p13 chr16: 1,846,555-2,190,441 NTHL1, MSRB1, 29 more genes
    nsv6959164copy number variation1nstd229human GRCh38 chr16: 1,882,476-2,224,508 , GRCh37.p13 chr16: 1,932,477-2,274,509 SNORD60, NTHL1, 35 more genes
    nsv6958935copy number variation1nstd229human GRCh38 chr16: 1,975,501-2,237,700 , GRCh37.p13 chr16: 2,025,502-2,287,701 BRICD5, MLST8, 25 more genes
    nsv6637964copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,146,432 , GRCh38.p12 chr16: 1,971,143-2,096,431 NTHL1, SYNGR3, 11 more genes
    nsv6637768copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054 CRAMP1, LOC105371046, 57 more genes
    nsv6637664copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,266,791 , GRCh38.p12 chr16: 1,971,143-2,216,790 SNHG19, MIR6511B1, 22 more genes
    nsv6637330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,942,430-2,653,144 , GRCh38.p12 chr16: 1,892,429-2,603,143 SNHG19, SNHG9, 58 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
    nsv6595307inversion1nstd223human GRCh38 chr16: 1,516,512-2,069,676 , GRCh37.p13 chr16: 1,566,513-2,119,677 MAPK8IP3-AS1, EME2, 37 more genes
    nsv6511034copy number variation1nstd223human GRCh38 chr16: 1,969,797-1,973,336 , GRCh37.p13 chr16: 2,019,798-2,023,337 TBL3
    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