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 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099187copy number variation1nstd231human GRCh38.p12 chr1: 24,354,009-27,158,528 , GRCh37 chr1: 24,680,499-27,485,019 RUNX3, CD52, 88 more genes
    nsv7096043copy number variation1nstd102humanPathogenic GRCh37 chr1: 26,784,272-26,795,632 , GRCh38.p12 chr1: 26,457,781-26,469,141 DHDDS-AS1, DHDDS
    nsv7095609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 25,870,190-27,278,871 , GRCh38.p12 chr1: 25,543,699-26,952,380 RPL34P4, GPATCH3, 53 more genes
    nsv7095524copy number variation1nstd102humanPathogenic GRCh37 chr1: 26,757,796-26,764,723 , GRCh38.p12 chr1: 26,431,305-26,438,232 DHDDS
    nsv7093211copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 26,784,388-26,784,449 , GRCh38 chr1: 26,457,897-26,457,958 DHDDS
    nsv7050797inversion1nstd229human GRCh38 chr1: 26,427,803-26,431,702 , GRCh37.p13 chr1: 26,754,294-26,758,193 LIN28A, DHDDS
    nsv7048473inversion1nstd229human GRCh38 chr1: 26,427,871-26,431,630 , GRCh37.p13 chr1: 26,754,362-26,758,121 LIN28A, DHDDS
    nsv7048036inversion1nstd229human GRCh38 chr1: 25,582,347-26,624,382 , GRCh37.p13 chr1: 25,908,838-26,950,873 MAN1C1, DHDDS-AS1, 41 more genes
    nsv7046480inversion1nstd229human GRCh38 chr1: 25,582,465-26,624,179 , GRCh37.p13 chr1: 25,908,956-26,950,670 SNRPFP2, ZPLD2P, 41 more genes
    nsv6648045copy number variation1nstd229human GRCh38 chr1: 26,400,001-27,138,900 , GRCh37.p13 chr1: 26,726,492-27,465,391 RN7SL679P, NR0B2, 26 more genes
    nsv6647799copy number variation1nstd229human GRCh38 chr1: 25,804,801-26,645,100 , GRCh37.p13 chr1: 26,131,292-26,971,591 RPL17P9, MIR3917, 39 more genes
    nsv6647599copy number variation1nstd229human GRCh38 chr1: 26,448,498-26,449,127 , GRCh37.p13 chr1: 26,774,989-26,775,618 DHDDS
    nsv6647354copy number variation1nstd229human GRCh38 chr1: 26,095,901-27,680,900 , GRCh37.p13 chr1: 26,422,392-28,007,411 ZPLD2P, CEP85, 65 more genes
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6554227inversion1nstd223human GRCh38 chr1: 26,436,600-26,437,051 , GRCh37.p13 chr1: 26,763,091-26,763,542 DHDDS
    nsv6537920inversion1nstd223human GRCh38 chr1: 26,451,882-26,452,837 , GRCh37.p13 chr1: 26,778,373-26,779,328 DHDDS, RPL17P9
    nsv6333556copy number variation1nstd223human GRCh38 chr1: 24,890,501-27,921,300 , GRCh37.p13 chr1: 25,216,992-28,247,811 RUNX3, MACO1, 108 more genes
    nsv6322238copy number variation1nstd223human GRCh38 chr1: 26,448,497-26,449,126 , GRCh37.p13 chr1: 26,774,988-26,775,617 DHDDS
    nsv6321465copy number variation1nstd223human GRCh38 chr1: 26,433,986-26,436,002 , GRCh37.p13 chr1: 26,760,477-26,762,493 DHDDS
    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