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 1552

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2673642copy number variation50estd199human GRCh37 chrX: 91,853,345-91,909,992 , GRCh38.p12 chrX: 92,598,346-92,654,993 PCDH11X
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2676626copy number variation15estd199human GRCh37 chr18: 65,295,573-65,317,246 , GRCh38.p12 chr18: 67,628,336-67,650,009 DSEL-AS1
    esv2673531copy number variation4estd199human GRCh37 chr4: 65,819,569-65,841,219 , GRCh38.p12 chr4: 64,953,851-64,975,501 LINC02232
    esv2660895copy number variation4estd199human GRCh37 chr4: 65,819,739-65,841,187 , GRCh38.p12 chr4: 64,954,021-64,975,469 LINC02232
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2671157copy number variation55estd199human GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160 LOC105377865
    esv2662905copy number variation26estd199human GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160 LOC105377865
    esv2676907copy number variation19estd199human GRCh37 chr5: 155,577,191-155,591,407 , GRCh38.p12 chr5: 156,150,181-156,164,397 SGCD
    esv2660310copy number variation1estd199human GRCh37 chr14: 89,345,272-89,359,023 , GRCh38.p12 chr14: 88,878,928-88,892,679 TTC8
    esv2658691copy number variation5estd199human GRCh37 chr12: 127,591,889-127,604,369 , GRCh38.p12 chr12: 127,107,344-127,119,824 , GRCh38.p12 chr12|NW_019805499.1: 53,868-66,348 LOC107984449
    esv2665413copy number variation30estd199human GRCh37 chr8: 63,214,945-63,226,892 , GRCh38.p12 chr8: 62,302,386-62,314,333 NKAIN3
    esv2670295copy number variation118estd199human GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754 ZBTB20
    esv2660593copy number variation56estd199human GRCh37 chrX: 91,610,345-91,620,792 , GRCh38.p12 chrX: 92,355,346-92,365,793 PCDH11X
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    esv2675328copy number variation4estd199human GRCh37 chr2: 128,103,654-128,114,045 , GRCh38.p12 chr2: 127,346,078-127,356,469 MAP3K2
    esv2657240copy number variation60estd199human GRCh37 chr8: 63,215,349-63,225,227 , GRCh38.p12 chr8: 62,302,790-62,312,668 NKAIN3
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2657546copy number variation14estd199human GRCh37 chr20: 15,310,946-15,320,655 , GRCh38.p12 chr20: 15,330,300-15,340,009 MACROD2
    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