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 384

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099206copy number variation1nstd231human GRCh38.p12 chr1: 54,693,460-58,571,894 , GRCh37 chr1: 55,159,133-59,037,566 C8A, C8B, 49 more genes
    nsv7095996copy number variation1nstd102humanUncertain significance GRCh37 chr1: 55,223,407-55,352,792 , GRCh38.p12 chr1: 54,757,734-54,887,119 CIMAP2, DHCR24, 3 more genes
    nsv7053230inversion1nstd229human GRCh38 chr1: 54,133,615-56,561,151 , GRCh37.p13 chr1: 54,599,288-57,026,824 GOT2P1, CIMAP2, 41 more genes
    nsv6651985copy number variation1nstd229human GRCh38 chr1: 54,835,601-54,840,300 , GRCh37.p13 chr1: 55,301,274-55,305,973 CIMAP2
    nsv6651984copy number variation1nstd229human GRCh38 chr1: 54,821,878-54,822,196 , GRCh37.p13 chr1: 55,287,551-55,287,869 CIMAP2
    nsv6651972copy number variation1nstd229human GRCh38 chr1: 54,835,339-54,839,898 , GRCh37.p13 chr1: 55,301,012-55,305,571 CIMAP2
    nsv6651971copy number variation1nstd229human GRCh38 chr1: 54,824,301-54,827,600 , GRCh37.p13 chr1: 55,289,974-55,293,273 CIMAP2
    nsv6651970copy number variation1nstd229human GRCh38 chr1: 54,774,260-54,865,477 , GRCh37.p13 chr1: 55,239,933-55,331,150 TTC22, CIMAP2, 1 more genes
    nsv6651948copy number variation1nstd229human GRCh38 chr1: 54,489,332-54,940,292 , GRCh37.p13 chr1: 54,955,005-55,405,965 FAM151A, LINC02784, 12 more genes
    nsv6651885copy number variation1nstd229human GRCh38 chr1: 54,810,236-54,813,646 , GRCh37.p13 chr1: 55,275,909-55,279,319 CIMAP2
    nsv6651884copy number variation1nstd229human GRCh38 chr1: 54,798,403-55,085,262 , GRCh37.p13 chr1: 55,264,076-55,550,935 PCSK9, TTC22, 8 more genes
    nsv6651758copy number variation1nstd229human GRCh38 chr1: 54,736,701-54,817,700 , GRCh37.p13 chr1: 55,202,374-55,283,373 TTC22, MROH7-TTC4, 3 more genes
    nsv6651757copy number variation1nstd229human GRCh38 chr1: 54,736,660-54,808,304 , GRCh37.p13 chr1: 55,202,333-55,273,977 CIMAP2, TTC4, 3 more genes
    nsv6651227copy number variation1nstd229human GRCh38 chr1: 54,835,301-54,840,100 , GRCh37.p13 chr1: 55,300,974-55,305,773 CIMAP2
    nsv6651226copy number variation1nstd229human GRCh38 chr1: 54,819,696-54,830,980 , GRCh37.p13 chr1: 55,285,369-55,296,653 CIMAP2
    nsv6626459copy number variation1nstd224human GRCh37 chr1: 54,883,003-55,349,442 , GRCh38.p12 chr1: 54,417,330-54,883,769 DHCR24, FAM151A, 11 more genes
    nsv6626264copy number variation1nstd224human GRCh37 chr1: 55,203,135-55,273,670 , GRCh38.p12 chr1: 54,737,462-54,807,997 TTC4, PARS2, 3 more genes
    nsv6626263copy number variation1nstd224human GRCh37 chr1: 55,103,945-55,281,991 , GRCh38.p12 chr1: 54,638,272-54,816,318 TTC4, PARS2, 5 more genes
    nsv6626262copy number variation1nstd224human GRCh37 chr1: 54,887,297-55,324,869 , GRCh38.p12 chr1: 54,421,624-54,859,196 TALDO1P1, TTC4, 11 more genes
    nsv6626261copy number variation1nstd224human GRCh37 chr1: 54,854,079-55,339,086 , GRCh38.p12 chr1: 54,388,406-54,873,413 TALDO1P1, ACOT11, 12 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