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 111

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905756copy number variation1nstd209human GRCh38 chr5: 139,452,583-139,453,658 , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv5905335copy number variation1nstd209human GRCh38 chr5: 139,452,109-139,452,305 , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv5902272copy number variation1nstd209human GRCh38 chr5: 139,442,441-139,447,835 , GRCh37.p13 chr5: 138,778,130-138,783,524 RNU5B-4P, ECSCR
    nsv5901638copy number variation1nstd209human GRCh38 chr5: 139,452,444-139,453,828 , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv5841150copy number variation1nstd209human GRCh38 chr5: 139,442,492-139,447,425 , GRCh37.p13 chr5: 138,778,181-138,783,114 RNU5B-4P, ECSCR
    nsv5580683copy number variation1nstd207human GRCh38 chr5: 139,452,659-139,453,395 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv5459867copy number variation1nstd206human GRCh38 chr5: 139,442,441-139,447,841 , GRCh37.p13 chr5: 138,778,130-138,783,530 RNU5B-4P, ECSCR
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5368975translocation1nstd200human GRCh38 chr5: 139,452,658-139,452,658 , GRCh38 chr5: 139,453,659-139,453,659 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv5328618translocation1nstd204human GRCh38.p13 chr5: 139,452,658-139,452,658 , GRCh38.p13 chr5: 139,453,659-139,453,659 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 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
    nsv4938873copy number variation1nstd200human GRCh38 chr5: 139,450,884-139,461,446 , GRCh37.p13 chr: NaN-NaN ECSCR
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805862copy number variation1nstd200human GRCh37 chr5: 138,778,130-138,783,530 , GRCh38.p12 chr5: 139,442,441-139,447,841 ECSCR, RNU5B-4P
    nsv4769371copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 137,754,277-138,994,590 , GRCh38.p12 chr5: 138,418,588-139,615,005 CTNNA1, EGR1, 36 more genes
    nsv4729564copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,351,402-138,893,343 , GRCh38.p12 chr5: 139,015,713-139,513,758 PROB1, SNORA74A, 19 more genes
    nsv4729431copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,101,724-138,876,953 , GRCh38.p12 chr5: 138,766,035-139,497,368 PROB1, NCOA4P4, 22 more genes
    nsv4456012copy number variation1nstd102humanPathogenic GRCh37 chr5: 137,865,800-139,097,368 , GRCh38.p12 chr5: 138,530,111-139,717,783 SNORD63, ECSCR, 36 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
    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