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 14544

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1174686copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr2: 138,279,976-138,551,278 , GRCh38.p12 chr2: 137,522,406-137,793,708 THSD7B
    nsv1180509copy number variation220nstd112Neandertal, Denisova hominin, human GRCh37 chr9: 11,729,801-11,979,781 , GRCh38.p12 chr9: 11,729,801-11,979,781 LOC101929446
    nsv1179604copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr8: 116,215,934-116,443,804 , GRCh38.p12 chr8: 115,203,705-115,431,576 TRPS1
    nsv1174221copy number variation225nstd112Neandertal, Denisova hominin, human GRCh37 chr2: 4,335,435-4,561,548 , GRCh38.p12 chr2: 4,287,845-4,513,958 NPM1P48
    nsv1173962copy number variation218nstd112Neandertal, Denisova hominin, human GRCh37 chr1: 189,325,460-189,544,615 , GRCh38.p12 chr1: 189,356,330-189,575,485 LOC105371657
    nsv1174437copy number variation224nstd112Neandertal, Denisova hominin, human GRCh37 chr2: 51,280,423-51,486,442 , GRCh38.p12 chr2: 51,053,285-51,259,304 NRXN1-DT
    nsv1181418copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr10: 117,037,654-117,234,987 , GRCh38.p12 chr10: 115,278,144-115,475,477 ATRNL1
    nsv1179894copy number variation158nstd112Denisova hominin, human GRCh37 chr9: 104,710,425-104,901,696 , GRCh38.p12 chr9: 101,948,143-102,139,414 ARL2BPP7
    nsv1176519copy number variation224nstd112Neandertal, Denisova hominin, human GRCh37 chr4: 168,808,123-168,995,942 , GRCh38.p12 chr4: 167,886,972-168,074,791 LOC105377523
    nsv1180118copy number variation224nstd112Neandertal, Denisova hominin, human GRCh37 chr8: 137,680,087-137,862,511 , GRCh38.p12 chr8: 136,667,844-136,850,268 LINC02055
    nsv1187667copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chrX: 6,450,477-6,630,171 , GRCh38.p12 chrX: 6,532,436-6,712,130 VCX3A
    nsv1187223copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chrX: 33,151,538-33,330,828 , GRCh38.p12 chrX: 33,133,421-33,312,711 DMD
    nsv1178830copy number variation224nstd112Neandertal, Denisova hominin, human GRCh37 chr6: 162,037,389-162,198,324 , GRCh38.p12 chr6: 161,616,357-161,777,292 PRKN
    nsv1176684copy number variation225nstd112Neandertal, Denisova hominin, human GRCh37 chr5: 99,504,873-99,665,445 , GRCh38.p12 chr5: 100,169,169-100,329,741 LOC105379101
    nsv1180429copy number variation218nstd112Neandertal, Denisova hominin, human GRCh37 chr9: 12,022,467-12,176,297 , GRCh38.p12 chr9: 12,022,467-12,176,297 LOC105375976
    nsv1174447copy number variation217nstd112Neandertal, Denisova hominin, human GRCh37 chr1: 189,197,426-189,347,296 , GRCh38.p12 chr1: 189,228,295-189,378,166 LOC105371657
    nsv1180027copy number variation219nstd112Neandertal, Denisova hominin, human GRCh37 chr9: 11,990,415-12,136,164 , GRCh38.p12 chr9: 11,990,415-12,136,164 LOC105375976
    nsv1181373copy number variation224nstd112Neandertal, Denisova hominin, human GRCh37 chr10: 68,449,653-68,592,005 , GRCh38.p12 chr10: 66,689,895-66,832,247 CTNNA3
    nsv1175697copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr3: 76,261,893-76,401,678 , GRCh38.p12 chr3: 76,212,742-76,352,527 ROBO2
    nsv1177975copy number variation225nstd112Neandertal, Denisova hominin, human GRCh37 chr6: 91,988,661-92,123,292 , GRCh38.p12 chr6: 91,278,943-91,413,574 LOC107986624
    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