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 170

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7137202copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,713,854-124,105,184 , GRCh38.p12 chr6: 112,392,652-123,784,039 COL10A1, FABP7, 129 more genes
    nsv7097176copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,441,236-119,252,888 , GRCh38.p12 chr6: 116,120,073-118,931,723 RN7SKP18, COL10A1, 49 more genes
    nsv7051708inversion1nstd229human GRCh38 chr6: 115,507,946-121,145,291 , GRCh37.p13 chr6: 115,829,110-121,466,437 COL10A1, KRT18P22, 67 more genes
    nsv7043912inversion1nstd229human GRCh38 chr6: 113,606,593-119,197,751 , GRCh37.p13 chr6: 113,927,795-119,518,916 TPI1P3, CALHM5, 73 more genes
    nsv6811986copy number variation1nstd229human GRCh38 chr6: 116,745,265-116,750,466 , GRCh37.p13 chr6: 117,066,428-117,071,629 FAM162B
    nsv6811923copy number variation1nstd229human GRCh38 chr6: 116,638,417-116,840,094 , GRCh37.p13 chr6: 116,959,580-117,161,257 LOC105377963, KPNA5, 3 more genes
    nsv6807421copy number variation1nstd229human GRCh38 chr6: 116,748,521-116,750,514 , GRCh37.p13 chr6: 117,069,684-117,071,677 FAM162B
    nsv6803276copy number variation1nstd229human GRCh38 chr6: 116,692,013-116,806,077 , GRCh37.p13 chr6: 117,013,176-117,127,240 KPNA5, LOC105377963, 2 more genes
    nsv6606808copy number variation1nstd223human GRCh38 chr6: 111,642,175-118,933,374 , GRCh37.p13 chr6: 111,963,378-119,254,539 COL10A1, LOC105377952, 106 more genes
    nsv6602805copy number variation1nstd223human GRCh38 chr6: 116,748,521-116,750,510 , GRCh37.p13 chr6: 117,069,684-117,071,673 FAM162B
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313764copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,944,106-117,228,916 , GRCh38.p12 chr6: 116,622,943-116,907,753 FAM162B, RSPH4A, 5 more genes
    nsv6313666copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,212,698-119,482,708 , GRCh38.p12 chr6: 115,891,534-119,161,543 FAM184A, LOC107986523, 53 more genes
    nsv6312019copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,937,787-117,252,669 , GRCh38.p12 chr6: 116,616,624-116,931,506 RFX6, RSPH4A, 5 more genes
    nsv6301726copy number variation1nstd186human GRCh37 chr6: 117,069,684-117,071,673 , GRCh38.p12 chr6: 116,748,521-116,750,510 FAM162B
    nsv6136164copy number variation1nstd213human GRCh37 chr6: 116,520,000-117,620,001 , GRCh38.p12 chr6: 116,198,837-117,298,838 COL10A1, KPNA5, 26 more genes
    nsv5894194copy number variation1nstd209human GRCh38 chr6: 116,748,518-116,750,509 , GRCh37.p13 chr6: 117,069,681-117,071,672 FAM162B
    nsv5843720copy number variation1nstd209human GRCh38 chr6: 116,748,502-116,750,524 , GRCh37.p13 chr6: 117,069,665-117,071,687 FAM162B
    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