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 1638

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2658503copy number variation100estd199human GRCh37 chr6: 32,454,245-32,508,892 , GRCh38.p12 chr6: 32,486,468-32,541,115 HLA-DRB5
    esv2676879copy number variation198estd199human GRCh37 chr4: 34,779,980-34,829,038 , GRCh38.p12 chr4: 34,778,358-34,827,416 , GRCh38.p12 chr4|NW_003315915.1: 270,687-319,745 LOC105378262
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2665540copy number variation104estd199human GRCh37 chr22: 17,240,645-17,278,192 , GRCh38.p12 chr22: 16,759,755-16,797,302 XKR3
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2661915copy number variation81estd199human GRCh37 chr6: 77,437,226-77,458,987 , GRCh38.p12 chr6: 76,727,509-76,749,270 LOC105377861
    esv2660999copy number variation147estd199human GRCh37 chr1: 169,224,745-169,246,292 , GRCh38.p12 chr1: 169,255,507-169,277,054 NME7
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2667383copy number variation138estd199human GRCh37 chr2: 98,139,645-98,158,592 , GRCh38.p12 chr2: 97,523,182-97,542,129 ANKRD36B
    esv2671576copy number variation156estd199human GRCh37 chr7: 100,326,645-100,341,192 , GRCh38.p12 chr7: 100,729,022-100,743,569 ZAN
    esv2662211copy number variation1estd199human GRCh37 chr10: 97,425,933-97,439,582 , GRCh38.p12 chr10: 95,666,176-95,679,825 TCTN3
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2664165copy number variation220estd199human GRCh37 chr7: 100,327,572-100,340,716 , GRCh38.p12 chr7: 100,729,949-100,743,093 ZAN
    esv2659146copy number variation109estd199human GRCh37 chrX: 154,790,189-154,803,312 , GRCh38.p12 chrX: 155,560,528-155,573,651 TMLHE
    esv2670748copy number variation204estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2675345copy number variation1estd199human GRCh37 chr6: 22,001,121-22,013,216 , GRCh38.p12 chr6: 22,000,892-22,012,987 CASC15
    esv2667550copy number variation9estd199human GRCh37 chr8: 60,996,549-61,007,774 , GRCh38.p12 chr8: 60,083,990-60,095,215 LOC105375861
    esv2663832copy number variation109estd199human GRCh37 chr4: 118,579,966-118,591,119 , GRCh38.p12 chr4: 117,658,811-117,669,964 LINC01378
    esv2663949copy number variation47estd199human GRCh37 chr20: 52,647,064-52,658,002 , GRCh38.p12 chr20: 54,030,525-54,041,463 BCAS1
    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