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 1334

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2666047copy number variation7estd199human GRCh37 chr5: 17,527,013-17,606,098 , GRCh38.p12 chr5: 17,526,904-17,605,989 TAF11L6
    esv2657096copy number variation12estd199human GRCh37 chr11: 50,366,415-50,416,213 , GRCh38.p12 chr11: 50,407,244-50,457,042 LOC646813
    esv2677913copy number variation4estd199human GRCh37 chr10: 56,950,010-56,996,736 , GRCh38.p12 chr10: 55,190,250-55,236,976 PCDH15
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2676981copy number variation78estd199human GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922 CYP2A6
    esv2670476copy number variation17estd199human GRCh37 chr11: 21,187,109-21,215,852 , GRCh38.p12 chr11: 21,165,563-21,194,306 NELL1
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2672907copy number variation61estd199human GRCh37 chr13: 69,244,702-69,268,757 , GRCh38.p12 chr13: 68,670,570-68,694,625 RN7SL761P
    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
    esv2671157copy number variation55estd199human GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160 LOC105377865
    esv2662873copy number variation30estd199human GRCh37 chr8: 75,311,432-75,330,080 , GRCh38.p12 chr8: 74,399,197-74,417,845 GDAP1
    esv2672554copy number variation26estd199human GRCh37 chr8: 75,312,945-75,330,192 , GRCh38.p12 chr8: 74,400,710-74,417,957 GDAP1
    esv2664362copy number variation25estd199human GRCh37 chr8: 2,251,326-2,267,068 , GRCh38.p12 chr8|NT_187576.1: 486,536-502,278 LOC105377783
    esv2675305copy number variation21estd199human GRCh37 chr22: 28,186,245-28,200,392 , GRCh38.p12 chr22: 27,790,257-27,804,404 MN1
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2671527copy number variation6estd199human GRCh37 chr1: 210,601,359-210,614,183 , GRCh38.p12 chr1: 210,428,015-210,440,839 , GRCh38.p12 chr1|NW_011332687.1: 207,757-220,581 HHAT
    esv2656642copy number variation44estd199human GRCh37 chr8: 16,262,051-16,274,684 , GRCh38.p12 chr8: 16,404,542-16,417,175 LOC101929028
    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