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 663

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057143inversion1nstd229human GRCh38 chr2: 62,843,859-62,861,004 , GRCh37.p13 chr2: 63,070,994-63,088,139 EHBP1
    nsv7053969inversion1nstd229human GRCh38 chr2: 62,820,730-62,824,632 , GRCh37.p13 chr2: 63,047,865-63,051,767 EHBP1
    nsv7047174inversion1nstd229human GRCh38 chr2: 62,795,116-62,809,573 , GRCh37.p13 chr2: 63,022,251-63,036,708 EHBP1
    nsv7046314inversion1nstd229human GRCh38 chr2: 62,652,321-62,699,787 , GRCh37.p13 chr2: 62,879,456-62,926,922 EHBP1
    nsv6677221copy number variation1nstd229human GRCh38 chr2: 62,974,047-62,979,985 , GRCh37.p13 chr2: 63,201,182-63,207,120 EHBP1
    nsv6676675copy number variation1nstd229human GRCh38 chr2: 62,852,001-62,865,400 , GRCh37.p13 chr2: 63,079,136-63,092,535 EHBP1
    nsv6676317copy number variation1nstd229human GRCh38 chr2: 62,905,701-62,911,900 , GRCh37.p13 chr2: 63,132,836-63,139,035 EHBP1
    nsv6675380copy number variation1nstd229human GRCh38 chr2: 62,781,121-62,781,878 , GRCh37.p13 chr2: 63,008,256-63,009,013 EHBP1
    nsv6674184copy number variation1nstd229human GRCh38 chr2: 62,966,798-62,966,885 , GRCh37.p13 chr2: 63,193,933-63,194,020 EHBP1
    nsv6673273copy number variation1nstd229human GRCh38 chr2: 63,014,729-63,017,916 , GRCh37.p13 chr2: 63,241,864-63,245,051 EHBP1
    nsv6673190copy number variation1nstd229human GRCh38 chr2: 62,882,093-62,890,757 , GRCh37.p13 chr2: 63,109,228-63,117,892 EHBP1
    nsv6672234copy number variation1nstd229human GRCh38 chr2: 62,921,588-62,926,022 , GRCh37.p13 chr2: 63,148,723-63,153,157 EHBP1
    nsv6672117copy number variation1nstd229human GRCh38 chr2: 62,847,694-63,079,332 , GRCh37.p13 chr2: 63,074,829-63,306,467 EHBP1-AS1, RPS20P9, 2 more genes
    nsv6671200copy number variation1nstd229human GRCh38 chr2: 61,917,934-63,365,574 , GRCh37.p13 chr2: 62,145,069-63,592,709 OTX1, RN7SL51P, 22 more genes
    nsv6670752copy number variation1nstd229human GRCh38 chr2: 62,752,780-62,752,807 , GRCh37.p13 chr2: 62,979,915-62,979,942 EHBP1
    nsv6670234copy number variation1nstd229human GRCh38 chr2: 62,981,267-62,984,471 , GRCh37.p13 chr2: 63,208,402-63,211,606 EHBP1
    nsv6669884copy number variation1nstd229human GRCh38 chr2: 62,820,964-62,821,097 , GRCh37.p13 chr2: 63,048,099-63,048,232 EHBP1
    nsv6667608copy number variation1nstd229human GRCh38 chr2: 62,963,806-62,963,988 , GRCh37.p13 chr2: 63,190,941-63,191,123 EHBP1
    nsv6667068copy number variation1nstd229human GRCh38 chr2: 62,917,129-62,917,302 , GRCh37.p13 chr2: 63,144,264-63,144,437 EHBP1
    nsv6666294copy number variation1nstd229human GRCh38 chr2: 62,685,115-62,693,304 , GRCh37.p13 chr2: 62,912,250-62,920,439 EHBP1
    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