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 180

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6447914copy number variation1nstd223human GRCh38 chr9: 39,780,901-39,819,300 , GRCh37.p13 chr9: 41,925,919-41,964,318 CNTNAP3P6, FGF7P3, 1 more genes
    nsv6443674copy number variation1nstd223human GRCh38 chr9: 39,801,601-39,823,900 , GRCh37.p13 chr9: 41,946,619-41,968,918 GLIDR, FGF7P3
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142583copy number variation1nstd206human GRCh38 chr9: 39,786,000-39,862,150 , GRCh37.p13 chr9: 41,931,018-42,007,168 GLIDR, FGF7P3
    nsv6141968copy number variation1nstd206human GRCh38 chr9: 39,690,000-39,900,000 , GRCh37.p13 chr9: 41,835,018-42,045,018 GLIDR, FAM88D, 6 more genes
    nsv5664563inversion1nstd207human GRCh38 chr9: 39,265,868-42,796,744 , GRCh37.p13 chr9: 42,792,885-46,287,854 , PTGER4P1, 95 more genes
    nsv5256838copy number variation1nstd204human GRCh38.p13 chr9: 39,803,301-39,808,200 , GRCh37.p13 chr9: 41,948,319-41,953,218 GLIDR
    nsv5254276copy number variation1nstd204human GRCh38.p13 chr9: 39,806,701-39,823,900 , GRCh37.p13 chr9: 41,951,719-41,968,918 FGF7P3, GLIDR
    nsv5251146copy number variation1nstd204human GRCh38.p13 chr9: 39,799,101-39,803,100 , GRCh37.p13 chr9: 41,944,119-41,948,118 GLIDR
    nsv5247106copy number variation1nstd204human GRCh38.p13 chr9: 39,788,701-39,839,700 , GRCh37.p13 chr9: 41,933,719-41,984,718 FGF7P3, GLIDR
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4730044inversion33nstd198human GRCh38 chr9: 39,599,468-41,573,547 , GRCh37.p13 chr: NaN-NaN , PTGER4P1, 59 more genes
    nsv4712169copy number variation1nstd195human GRCh37 chr9: 41,949,401-41,950,651 , GRCh38.p12 chr9: 39,804,383-39,805,633 GLIDR
    nsv4709726copy number variation1nstd195human GRCh37 chr9: 41,953,901-41,962,751 , GRCh38.p12 chr9: 39,808,883-39,817,733 GLIDR, FGF7P3
    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