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 790

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2676981copy number variation78estd199human GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922 CYP2A6
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2669175copy number variation12estd199human GRCh37 chr7: 149,863,195-149,881,292 , GRCh38.p12 chr7: 150,166,106-150,184,203 ACTR3C
    esv2672582copy number variation25estd199human GRCh37 chr10: 122,769,701-122,787,511 , GRCh38.p12 chr10: 121,010,188-121,027,998 LOC105378521
    esv2674647copy number variation204estd199human GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081 XKR4
    esv2670596copy number variation22estd199human GRCh37 chr4: 151,874,295-151,885,892 , GRCh38.p12 chr4: 150,953,143-150,964,740 LRBA
    esv2677965copy number variation40estd199human GRCh37 chr4: 92,073,713-92,084,451 , GRCh38.p12 chr4: 91,152,562-91,163,300 CCSER1
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2670098copy number variation35estd199human GRCh37 chr16: 76,661,500-76,671,078 , GRCh38.p12 chr16: 76,627,603-76,637,181 LINC02125
    esv2673496copy number variation79estd199human GRCh37 chr11: 5,873,984-5,883,493 , GRCh38.p12 chr11: 5,852,754-5,862,263 OR52E8
    esv2668940copy number variation193estd199human GRCh37 chr12: 99,793,947-99,802,770 , GRCh38.p12 chr12: 99,400,169-99,408,992 ANKS1B
    esv2678664copy number variation17estd199human GRCh37 chr4: 44,019,345-44,027,442 , GRCh38.p12 chr4: 44,017,328-44,025,425 LINC02475
    esv2677767copy number variation161estd199human GRCh37 chr4: 21,369,090-21,376,907 , GRCh38.p12 chr4: 21,367,467-21,375,284 KCNIP4
    esv2668452copy number variation609estd199human GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643 LOC105378113
    esv2664776copy number variation250estd199human GRCh37 chr3: 191,064,685-191,071,667 , GRCh38.p12 chr3: 191,346,896-191,353,878 CCDC50
    esv2673116copy number variation32estd199human GRCh37 chr10: 37,816,563-37,823,511 , GRCh38.p12 chr10: 37,527,635-37,534,583 TACC1P1
    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