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 388

    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
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7073913inversion1nstd229human GRCh38 chr16: 1,683,909-1,796,668 , GRCh37.p13 chr16: 1,733,910-1,846,669 JPT2, SPSB3, 8 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
    nsv6974739copy number variation1nstd229human GRCh38 chr16: 1,791,101-1,793,300 , GRCh37.p13 chr16: 1,841,102-1,843,301 IGFALS
    nsv6969358copy number variation1nstd229human GRCh38 chr16: 1,771,177-1,825,934 , GRCh37.p13 chr16: 1,821,178-1,875,935 HAGH, NUBP2, 6 more genes
    nsv6965261copy number variation1nstd229human GRCh38 chr16: 1,351,958-1,810,245 , GRCh37.p13 chr16: 1,401,959-1,860,246 JPT2, UNKL, 26 more genes
    nsv6962654copy number variation1nstd229human GRCh38 chr16: 1,787,240-1,796,772 , GRCh37.p13 chr16: 1,837,241-1,846,773 IGFALS, NUBP2
    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
    nsv6635839copy number variation2nstd227human GRCh38.p12 chr16: 1,749,406-1,792,208 , GRCh37 chr16: 1,799,407-1,842,209 IGFALS, NME3, 5 more genes
    nsv6635834copy number variation1nstd227human GRCh38.p12 chr16: 1,754,034-1,792,208 , GRCh37 chr16: 1,804,035-1,842,209 IGFALS, NME3, 5 more genes
    nsv6635706copy number variation4nstd227human GRCh38.p12 chr16: 1,752,231-1,792,208 , GRCh37 chr16: 1,802,232-1,842,209 IGFALS, NME3, 5 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
    nsv6623189copy number variation1nstd224human GRCh37 chr16: 1,840,741-1,859,345 , GRCh38.p12 chr16: 1,790,740-1,809,344 HAGH, IGFALS
    nsv6595307inversion1nstd223human GRCh38 chr16: 1,516,512-2,069,676 , GRCh37.p13 chr16: 1,566,513-2,119,677 MAPK8IP3-AS1, EME2, 37 more genes
    nsv6503347copy number variation1nstd223human GRCh38 chr16: 1,763,672-1,867,909 , GRCh37.p13 chr16: 1,813,673-1,917,910 MEIOB, MAPK8IP3, 8 more genes
    nsv6307002copy number variation1nstd186human GRCh37 chr16: 1,837,241-1,846,776 , GRCh38.p12 chr16: 1,787,240-1,796,775 NUBP2, IGFALS
    nsv6306623copy number variation1nstd186human GRCh37 chr16: 1,821,001-1,871,001 , GRCh38.p12 chr16: 1,771,000-1,821,000 HAGH, IGFALS, 5 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