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 110

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673753copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr5: 131,893,017-131,978,056 , GRCh38.p12 chr5: 132,557,325-132,642,364 IL5, RAD50, 1 more genes
    nsv5673752copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,891,616-131,981,313 , GRCh38.p12 chr5: 132,555,924-132,645,621 IL5, RAD50, 1 more genes
    nsv5673578copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,893,011-131,978,062 , GRCh38.p12 chr5: 132,557,319-132,642,370 TH2LCRR, IL5, 1 more genes
    nsv5673509copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 131,973,767-131,973,921 , GRCh38.p12 chr5: 132,638,075-132,638,229 RAD50, TH2LCRR
    nsv5469329copy number variation1nstd206human GRCh38 chr5: 132,631,238-132,631,398 , GRCh37.p13 chr5: 131,966,930-131,967,090 RAD50, TH2LCRR
    nsv5455079copy number variation1nstd206human GRCh38 chr5: 132,656,249-132,656,731 , GRCh37.p13 chr5: 131,991,941-131,992,423 TH2LCRR, IL13
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4938606copy number variation1nstd200human GRCh38 chr5: 132,645,687-132,650,501 , GRCh37.p13 chr5: 131,981,379-131,986,193 TH2LCRR, RAD50
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4681922copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,972,797-131,973,925 , GRCh38.p12 chr5: 132,637,105-132,638,233 RAD50, TH2LCRR
    nsv4490516mobile element insertion1nstd166human GRCh37.p13 chr5: 131,991,219-131,991,219 , GRCh38.p12 chr5: 132,655,527-132,655,527 IL13, TH2LCRR
    nsv4450167copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,911,459-131,978,066 , GRCh38 chr5: 132,575,767-132,642,374 TH2LCRR, RAD50
    nsv4450053copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,893,007-131,978,066 , GRCh38 chr5: 132,557,315-132,642,374 RAD50, TH2LCRR, 1 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 ACTBP4, CAMLG, 157 more genes
    nsv3961082copy number variation1nstd168human GRCh38 chr5: 132,629,025-132,651,620 , GRCh37.p13 chr5: 131,964,717-131,987,312 TH2LCRR, RAD50
    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