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 1394

    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
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2669673copy number variation1estd199human GRCh37 chr1: 176,590,628-176,613,320 , GRCh38.p12 chr1: 176,621,492-176,644,184 PAPPA2
    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
    esv2678880copy number variation28estd199human GRCh37 chr13: 25,160,669-25,177,071 , GRCh38.p12 chr13: 24,586,531-24,602,933 TPTE2P6
    esv2675775copy number variation27estd199human GRCh37 chr9: 514,141-527,931 , GRCh38.p12 chr9: 514,141-527,931 KANK1
    esv2668652copy number variation25estd199human GRCh37 chr1: 111,377,295-111,389,642 , GRCh38.p12 chr1: 110,834,673-110,847,020 NRBF2P3
    esv2670295copy number variation118estd199human GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754 ZBTB20
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    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
    esv2666144copy number variation73estd199human GRCh37 chr17: 77,992,012-78,000,841 , GRCh38.p12 chr17: 80,018,213-80,027,042 TBC1D16
    esv2661167copy number variation22estd199human GRCh37 chr5: 20,419,692-20,428,474 , GRCh38.p12 chr5: 20,419,583-20,428,365 CDH18
    esv2676292copy number variation118estd199human GRCh37 chr1: 72,755,692-72,764,074 , GRCh38.p12 chr1: 72,290,009-72,298,391 , GRCh38.p12 chr1|NW_018654707.1: 2,276-10,658 LOC105378797
    esv2664189copy number variation25estd199human GRCh37 chr10: 75,374,045-75,382,242 , GRCh38.p12 chr10: 73,614,287-73,622,484 USP54
    esv2665629copy number variation18estd199human GRCh37 chr13: 92,386,745-92,394,392 , GRCh38.p12 chr13: 91,734,491-91,742,138 GPC5
    esv2657498copy number variation116estd199human GRCh37 chr4: 21,160,045-21,167,592 , GRCh38.p12 chr4: 21,158,422-21,165,969 KCNIP4
    esv2668452copy number variation609estd199human GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643 LOC105378113
    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