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 134

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078008inversion1nstd229human GRCh38 chr14: 60,214,891-67,756,686 , GRCh37.p13 chr14: 60,681,609-68,223,403 ATP6V1D, LOC101927756, 129 more genes
    nsv7077538inversion1nstd229human GRCh38 chr14: 63,703,374-67,849,523 , GRCh37.p13 chr14: 64,170,092-68,316,240 RPPH1-2P, SYNE2, 75 more genes
    nsv7077051inversion1nstd229human GRCh38 chr14: 63,334,072-65,942,752 , GRCh37.p13 chr14: 63,800,790-66,409,470 FNTB, PPP1R36, 53 more genes
    nsv7059243inversion1nstd229human GRCh38 chr14: 63,034,368-65,530,331 , GRCh37.p13 chr14: 63,501,086-65,997,049 MIR4706, RNU7-116P, 56 more genes
    nsv6977506copy number variation1nstd229human GRCh38 chr14: 62,671,855-65,773,169 , GRCh37.p13 chr14: 63,138,573-66,239,887 KCNH5, CHURC1-FNTB, 56 more genes
    nsv6975736copy number variation1nstd229human GRCh38 chr14: 64,941,840-64,997,986 , GRCh37.p13 chr14: 65,408,558-65,464,704 LOC107984655, FNTB, 3 more genes
    nsv6971934copy number variation1nstd229human GRCh38 chr14: 64,969,354-64,969,560 , GRCh37.p13 chr14: 65,436,072-65,436,278 CHURC1-FNTB, RAB15
    nsv6970803copy number variation1nstd229human GRCh38 chr14: 64,806,202-65,096,663 , GRCh37.p13 chr14: 65,272,920-65,563,381 CHURC1, MIR4706, 10 more genes
    nsv6964921copy number variation1nstd229human GRCh38 chr14: 64,954,866-64,961,093 , GRCh37.p13 chr14: 65,421,584-65,427,811 RAB15, CHURC1-FNTB
    nsv6961947copy number variation1nstd229human GRCh38 chr14: 64,961,041-64,961,085 , GRCh37.p13 chr14: 65,427,759-65,427,803 CHURC1-FNTB, RAB15
    nsv6960520copy number variation1nstd229human GRCh38 chr14: 64,700,079-65,240,524 , GRCh37.p13 chr14: 65,166,797-65,707,242 MAX, LINC02324, 15 more genes
    nsv6960104copy number variation1nstd229human GRCh38 chr14: 64,953,713-64,954,552 , GRCh37.p13 chr14: 65,420,431-65,421,270 CHURC1-FNTB, RAB15
    nsv6958265copy number variation1nstd229human GRCh38 chr14: 64,960,732-64,968,653 , GRCh37.p13 chr14: 65,427,450-65,435,371 CHURC1-FNTB, RAB15
    nsv6580445inversion1nstd223human GRCh38 chr14: 64,964,242-64,964,814 , GRCh37.p13 chr14: 65,430,960-65,431,532 CHURC1-FNTB, RAB15
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6315477copy number variation1nstd102humanUncertain significance GRCh37 chr14: 64,016,496-65,834,490 , GRCh38.p12 chr14: 63,549,778-65,367,772 LOC105370534, RNU7-116P, 43 more genes
    nsv6133134copy number variation1nstd213human GRCh37 chr14: 64,710,000-67,710,001 , GRCh38.p12 chr14: 64,243,282-67,243,284 ESR2, YBX1P1, 46 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5716695mobile element insertion1nstd211human GRCh38 chr14: 64,957,245-64,957,245 , GRCh37.p13 chr14: 65,423,963-65,423,963 CHURC1-FNTB, RAB15
    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