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 182

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099298copy number variation1nstd231human GRCh38.p12 chr1: 68,115,402-81,183,740 , GRCh37 chr1: 68,581,085-81,649,425 ACADM, COX6A1P1, 145 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7047632inversion1nstd229human GRCh38 chr1: 74,160,663-78,762,216 , GRCh37.p13 chr1: 74,626,347-79,227,901 SLC44A5, MGC27382, 66 more genes
    nsv6654960copy number variation1nstd229human GRCh38 chr1: 76,682,326-76,791,511 , GRCh37.p13 chr1: 77,148,011-77,257,196 LINC02567, TPI1P1, 1 more genes
    nsv6654957copy number variation1nstd229human GRCh38 chr1: 76,576,544-76,799,235 , GRCh37.p13 chr1: 77,042,229-77,264,920 ST6GALNAC3, LINC02567, 3 more genes
    nsv6654943copy number variation1nstd229human GRCh38 chr1: 76,312,312-77,024,659 , GRCh37.p13 chr1: 76,777,997-77,490,344 ST6GALNAC3, LINC02567, 5 more genes
    nsv6654722copy number variation1nstd229human GRCh38 chr1: 76,463,168-76,735,249 , GRCh37.p13 chr1: 76,928,853-77,200,934 ST6GALNAC3, LOC105378807, 1 more genes
    nsv6654716copy number variation1nstd229human GRCh38 chr1: 76,179,377-76,884,062 , GRCh37.p13 chr1: 76,645,062-77,349,747 LOC100418965, ST6GALNAC5, 5 more genes
    nsv6634835copy number variation1nstd227human GRCh38.p12 chr1: 76,646,366-77,027,004 , GRCh37 chr1: 77,112,051-77,492,689 ST6GALNAC5, TPI1P1, 2 more genes
    nsv6626281copy number variation1nstd224human GRCh37 chr1: 74,166,048-77,951,148 , GRCh38.p12 chr1: 73,700,365-77,485,463 ACADM, CRYZ, 41 more genes
    nsv6549621inversion1nstd223human GRCh38 chr1: 76,696,146-76,697,993 , GRCh37.p13 chr1: 77,161,831-77,163,678 TPI1P1
    nsv6328045copy number variation1nstd223human GRCh38 chr1: 76,669,245-76,938,262 , GRCh37.p13 chr1: 77,134,930-77,403,947 RNU6-161P, LINC02567, 2 more genes
    nsv6319391copy number variation1nstd223human GRCh38 chr1: 75,646,330-79,015,520 , GRCh37.p13 chr1: 76,112,015-79,481,205 ADGRL4, IFI44, 52 more genes
    nsv6315306copy number variation1nstd102humanUncertain significance GRCh38 chr1: 66,885,559-77,949,895 , GRCh37.p13 chr1: 67,351,242-78,415,580 DNAJB6P4, LRRC7, 137 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv5078797mobile element insertion1nstd203human GRCh38 chr1: 76,699,285-76,699,297 , GRCh37.p13 chr1: 77,164,970-77,164,982 TPI1P1
    nsv5069647mobile element insertion1nstd203human GRCh38 chr1: 76,699,287-76,699,297 , GRCh37.p13 chr1: 77,164,972-77,164,982 TPI1P1
    nsv5064636mobile element insertion1nstd203human GRCh38 chr1: 76,699,289-76,699,297 , GRCh37.p13 chr1: 77,164,974-77,164,982 TPI1P1
    nsv5063940mobile element insertion1nstd203human GRCh38 chr1: 76,699,257-76,699,297 , GRCh37.p13 chr1: 77,164,942-77,164,982 TPI1P1
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 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