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 366

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955489insertion1nstd209human GRCh38 chr1: 54,698,798-54,698,798 , GRCh37.p13 chr1: 55,164,471-55,164,471 MROH7-TTC4, MROH7
    nsv5886546copy number variation1nstd209human GRCh38 chr1: 54,658,531-54,685,414 , GRCh37.p13 chr1: 55,124,204-55,151,087 MROH7-TTC4, MROH7
    nsv5883218copy number variation1nstd209human GRCh38 chr1: 54,402,521-54,884,697 , GRCh37.p13 chr1: 54,868,194-55,350,370 MROH7, TTC22, 12 more genes
    nsv5869248copy number variation1nstd209human GRCh38 chr1: 54,582,624-54,789,779 , GRCh37.p13 chr1: 55,048,297-55,255,452 TTC4, PARS2, 5 more genes
    nsv5830395copy number variation1nstd209human GRCh38 chr1: 54,630,260-54,656,890 , GRCh37.p13 chr1: 55,095,933-55,122,563 MROH7-TTC4, ACOT11, 1 more genes
    nsv5830375copy number variation1nstd209human GRCh38 chr1: 54,682,443-54,691,724 , GRCh37.p13 chr1: 55,148,116-55,157,397 MROH7, MROH7-TTC4
    nsv5830260copy number variation1nstd209human GRCh38 chr1: 54,652,091-54,669,894 , GRCh37.p13 chr1: 55,117,764-55,135,567 MROH7, MROH7-TTC4
    nsv5725581mobile element insertion2nstd211human GRCh38 chr1: 54,658,625-54,658,625 , GRCh37.p13 chr1: 55,124,298-55,124,298 MROH7-TTC4, MROH7
    nsv5612505insertion1nstd207human GRCh38 chr1: 54,698,798-54,698,798 , GRCh37.p13 chr1: 55,164,471-55,164,471 MROH7-TTC4, MROH7
    nsv5562455mobile element insertion1nstd206human GRCh38 chr1: 54,658,625-54,658,676 , GRCh37.p13 chr1: 55,124,298-55,124,349 MROH7-TTC4, MROH7
    nsv5553733insertion1nstd206human GRCh38 chr1: 54,698,811-54,698,833 , GRCh37.p13 chr1: 55,164,484-55,164,506 MROH7-TTC4, MROH7
    nsv5430550copy number variation1nstd206human GRCh38 chr1: 54,674,569-54,674,902 , GRCh37.p13 chr1: 55,140,242-55,140,575 MROH7-TTC4, MROH7
    nsv5381135copy number variation1nstd102humanPathogenic GRCh37 chr1: 51,941,877-56,688,514 , GRCh38.p12 chr1: 51,476,205-56,222,842 LRP8-DT, LRRC42, 122 more genes
    nsv5361889translocation1nstd200human GRCh38 chr14: 22,636,354-22,636,354 , GRCh38 chr1: 54,706,384-54,706,384 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr1: 55,172,057-55,172,057 MROH7, MROH7-TTC4
    nsv5361886translocation1nstd200human GRCh38 chr1: 54,676,270-54,676,270 , GRCh38 chr1: 54,682,482-54,682,482 , GRCh37.p13 chr1: 55,141,943-55,141,943 , GRCh37.p13 chr1: 55,148,155-55,148,155 MROH7, MROH7-TTC4
    nsv5361881translocation1nstd200human GRCh38 chr1: 54,672,921-54,672,921 , GRCh38 chr1: 54,676,594-54,676,594 , GRCh37.p13 chr1: 55,138,594-55,138,594 , GRCh37.p13 chr1: 55,142,267-55,142,267 MROH7-TTC4, MROH7
    nsv5285983copy number variation1nstd204human GRCh37.p13 chr1: 55,148,374-55,379,984 , GRCh38.p13 chr1: 54,682,701-54,914,311 DHCR24, TTC4, 6 more genes
    nsv5217743copy number variation1nstd204human GRCh38.p13 chr1: 54,702,366-54,704,930 , GRCh37.p13 chr1: 55,168,039-55,170,603 MROH7-TTC4, MROH7
    nsv5200594copy number variation1nstd204human GRCh38.p13 chr1: 54,682,243-54,698,323 , GRCh37.p13 chr1: 55,147,916-55,163,996 MROH7-TTC4, MROH7
    nsv5200455copy number variation1nstd204human GRCh37.p13 chr1: 55,148,074-55,379,973 , GRCh38.p13 chr1: 54,682,401-54,914,300 DHCR24, TTC4, 6 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