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 773

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146157insertion1nstd232human GRCh37.p13 chr2: 159,191,006-159,191,006 , GRCh38.p12 chr2: 158,334,494-158,334,494 CCDC148
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7051705inversion1nstd229human GRCh38 chr2: 158,216,223-158,243,253 , GRCh37.p13 chr2: 159,072,735-159,099,765 CCDC148, CCDC148-AS1
    nsv7051336inversion1nstd229human GRCh38 chr2: 158,179,403-158,302,558 , GRCh37.p13 chr2: 159,035,915-159,159,070 CCDC148-AS1, CCDC148
    nsv7048724inversion1nstd229human GRCh38 chr2: 158,236,158-158,236,223 , GRCh37.p13 chr2: 159,092,670-159,092,735 CCDC148-AS1, CCDC148
    nsv7045930inversion1nstd229human GRCh38 chr2: 158,197,125-158,403,538 , GRCh37.p13 chr2: 159,053,637-159,260,050 CCDC148-AS1, CCDC148
    nsv7039524inversion1nstd229human GRCh38 chr2: 158,278,606-158,278,965 , GRCh37.p13 chr2: 159,135,118-159,135,477 CCDC148
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6697710copy number variation1nstd229human GRCh38 chr2: 158,405,857-158,407,901 , GRCh37.p13 chr2: 159,262,369-159,264,413 CCDC148
    nsv6697688copy number variation1nstd229human GRCh38 chr2: 158,350,697-158,360,892 , GRCh37.p13 chr2: 159,207,209-159,217,404 CCDC148
    nsv6697351copy number variation1nstd229human GRCh38 chr2: 157,835,146-158,258,896 , GRCh37.p13 chr2: 158,691,658-159,115,408 ACVR1, UPP2, 7 more genes
    nsv6696735copy number variation1nstd229human GRCh38 chr2: 158,205,874-158,207,053 , GRCh37.p13 chr2: 159,062,386-159,063,565 CCDC148-AS1, CCDC148
    nsv6696532copy number variation1nstd229human GRCh38 chr2: 158,385,338-158,385,420 , GRCh37.p13 chr2: 159,241,850-159,241,932 CCDC148
    nsv6696477copy number variation1nstd229human GRCh38 chr2: 158,279,449-158,397,509 , GRCh37.p13 chr2: 159,135,961-159,254,021 CCDC148
    nsv6693136copy number variation1nstd229human GRCh38 chr2: 158,441,222-158,451,335 , GRCh37.p13 chr2: 159,297,734-159,307,847 RN7SL393P, CCDC148
    nsv6692633copy number variation1nstd229human GRCh38 chr2: 158,454,026-158,570,939 , GRCh37.p13 chr2: 159,310,538-159,427,451 RPL7AP22, CCDC148, 1 more genes
    nsv6691737copy number variation1nstd229human GRCh38 chr2: 158,396,987-158,407,631 , GRCh37.p13 chr2: 159,253,499-159,264,143 CCDC148
    nsv6691585copy number variation1nstd229human GRCh38 chr2: 158,179,003-158,182,533 , GRCh37.p13 chr2: 159,035,515-159,039,045 CCDC148-AS1, CCDC148
    nsv6690719copy number variation1nstd229human GRCh38 chr2: 158,302,301-158,306,300 , GRCh37.p13 chr2: 159,158,813-159,162,812 CCDC148
    nsv6689423copy number variation1nstd229human GRCh38 chr2: 158,374,665-158,374,690 , GRCh37.p13 chr2: 159,231,177-159,231,202 CCDC148
    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