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 453

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7140705copy number variation1nstd232human GRCh37.p13 chr5: 196,752-196,835 , GRCh38.p12 chr5: 196,637-196,720 CCDC127, LRRC14B
    nsv7047634inversion1nstd229human GRCh38 chr5: 90,743-229,045 , GRCh37.p13 chr5: 90,858-229,160 CCDC127, LRRC14B, 2 more genes
    nsv7045728inversion1nstd229human GRCh38 chr5: 182,184-229,696 , GRCh37.p13 chr5: 182,299-229,811 CCDC127, LRRC14B, 2 more genes
    nsv7045668inversion1nstd229human GRCh38 chr5: 20,164-205,286 , GRCh37.p13 chr5: 20,164-205,401 CCDC127, LRRC14B, 3 more genes
    nsv7042391inversion1nstd229human GRCh38 chr5: 190,811-661,964 , GRCh37.p13 chr5: 190,926-662,079 LOC100310782, LOC105374606, 20 more genes
    nsv6777757copy number variation1nstd229human GRCh38 chr5: 187,616-194,807 , GRCh37.p13 chr5: 187,731-194,922 LRRC14B, PLEKHG4B
    nsv6776249copy number variation1nstd229human GRCh38 chr5: 191,265-303,477 , GRCh37.p13 chr5: 191,380-303,592 CCDC127, LRRC14B, 5 more genes
    nsv6775835copy number variation1nstd229human GRCh38 chr5: 190,701-192,200 , GRCh37.p13 chr5: 190,816-192,315 LRRC14B
    nsv6772296copy number variation1nstd229human GRCh38 chr5: 105,167-310,399 , GRCh37.p13 chr5: 105,282-310,514 SDHA, PDCD6-DT, 6 more genes
    nsv6771095copy number variation1nstd229human GRCh38 chr5: 117,534-592,796 , GRCh37.p13 chr5: 117,649-592,911 SDHA, CCDC127, 17 more genes
    nsv6770308copy number variation1nstd229human GRCh38 chr5: 194,424-306,338 , GRCh37.p13 chr5: 194,539-306,453 CCDC127, LRRC14B, 5 more genes
    nsv6769967copy number variation1nstd229human GRCh38 chr5: 142,402-197,874 , GRCh37.p13 chr5: 142,517-197,989 CCDC127, LRRC14B, 1 more genes
    nsv6769260copy number variation1nstd229human GRCh38 chr5: 129,691-222,565 , GRCh37.p13 chr5: 129,806-222,680 SDHA, CCDC127, 2 more genes
    nsv6762854copy number variation1nstd229human GRCh38 chr5: 95,146-200,737 , GRCh37.p13 chr5: 95,261-200,852 CCDC127, LRRC14B, 1 more genes
    nsv6760811copy number variation1nstd229human GRCh38 chr5: 191,264-191,326 , GRCh37.p13 chr5: 191,379-191,441 LRRC14B
    nsv6759769copy number variation1nstd229human GRCh38 chr5: 189,354-196,617 , GRCh37.p13 chr5: 189,469-196,732 LRRC14B, CCDC127, 1 more genes
    nsv6759682copy number variation1nstd229human GRCh38 chr5: 151,928-460,171 , GRCh37.p13 chr5: 152,043-460,286 PDCD6-AHRR, EXOC3-AS1, 10 more genes
    nsv6637091copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,265-668,842 , GRCh38.p12 chr5: 150,150-668,727 EXOC3, SLC9A3, 21 more genes
    nsv6636994copy number variation1nstd102humanUncertain significance GRCh37 chr5: 113,577-424,937 , GRCh38.p12 chr5: 113,462-424,822 AHRR, PDCD6-AHRR, 8 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