U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 398

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv4008929inversion1estd231human GRCh37 chr3: 1,474,325-1,666,423 , GRCh38.p12 chr3: 1,432,641-1,624,739 RPL23AP38
    esv4009086inversion1estd231human GRCh37 chr7: 152,574,763-152,760,109 , GRCh38.p12 chr7: 152,877,678-153,063,024 ACTR3B
    esv4009102inversion1estd231human GRCh38.p12 chr8: 139,498,146-139,600,717 , GRCh37 chr8: 140,510,389-140,612,960 KCNK9
    esv4008963inversion1estd231human GRCh38.p12 chr4: 18,175,378-18,269,869 , GRCh37 chr4: 18,177,001-18,271,492 LOC107986262
    esv4009271inversion1estd231human GRCh37 chr17: 2,333,706-2,415,892 , GRCh38.p12 chr17: 2,430,412-2,512,598 METTL16
    esv4008869inversion1estd231human GRCh38.p12 chr1: 159,458,825-159,525,200 , GRCh37 chr1: 159,428,615-159,494,990 LINC02819
    esv4008949inversion1estd231human GRCh37 chr3: 112,383,781-112,443,197 , GRCh38.p12 chr3: 112,664,934-112,724,350 MAT2AP1
    esv4009084inversion1estd231human GRCh37 chr7: 146,701,026-146,758,975 , GRCh38.p12 chr7: 147,003,934-147,061,883 CNTNAP2
    esv4009212inversion1estd231human GRCh38.p12 chr13: 42,457,884-42,511,668 , GRCh37 chr13: 43,032,020-43,085,804 LINC02341
    esv4009012inversion1estd231human GRCh37 chr5: 84,883,137-84,929,868 , GRCh38.p12 chr5: 85,587,319-85,634,050 LOC105379061
    esv4008917inversion1estd231human GRCh38.p12 chr2: 131,777,356-131,821,780 , GRCh37 chr2: 132,534,929-132,579,353 , GRCh38.p12 chr2|NT_187528.1: 81,417-110,099 CDRT15P3
    esv4008991inversion1estd231human GRCh38.p12 chr4: 170,319,172-170,361,221 , GRCh37 chr4: 171,240,323-171,282,372 LINC02512
    esv4008886inversion1estd231human GRCh38.p12 chr1: 247,129,683-247,169,561 , GRCh37 chr1: 247,292,985-247,332,863 ZNF124
    esv4008931inversion1estd231human GRCh37 chr3: 8,820,979-8,860,556 , GRCh38.p12 chr3: 8,779,293-8,818,870 LOC107986061
    esv4009295inversion1estd231human GRCh38.p12 chr19: 6,296,871-6,331,498 , GRCh37 chr19: 6,296,882-6,331,509 ACER1
    esv4008950inversion1estd231human GRCh37 chr3: 122,466,497-122,499,737 , GRCh38.p12 chr3: 122,747,650-122,780,890 HSPBAP1
    esv4009088inversion1estd231human GRCh37 chr7: 158,925,542-158,956,750 , GRCh38.p12 chr7: 159,132,851-159,164,059 VIPR2
    esv4009225inversion1estd231human GRCh38.p12 chr14: 44,032,377-44,063,362 , GRCh37 chr14: 44,501,580-44,532,565 LINC02307
    esv4008947inversion1estd231human GRCh37 chr3: 85,967,279-85,995,115 , GRCh38.p12 chr3: 85,918,129-85,945,965 CADM2
    esv4009273inversion1estd231human GRCh37 chr17: 3,661,872-3,688,654 , GRCh38.p12 chr17: 3,758,578-3,785,360 ITGAE
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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