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 82

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4384957copy number variation1nstd173human GRCh37 chr6: 102,769,217-102,954,531 , GRCh38.p12 chr6: 102,321,342-102,506,656 TARDBPP5
    nsv4383568copy number variation1nstd173human GRCh37 chr6: 168,835,089-169,009,966 , GRCh38.p12 chr6: 168,434,409-168,609,286 SMOC2
    nsv4380463copy number variation77nstd173human GRCh37 chr2: 98,118,115-98,162,176 , GRCh38.p12 chr2: 97,501,652-97,545,713 ANKRD36B
    nsv4378046copy number variation1nstd173human GRCh37 chr6: 169,996,740-170,036,260 , GRCh38.p12 chr6: 169,596,644-169,636,164 WDR27
    nsv4374011copy number variation1nstd173human GRCh37 chr6: 102,598,244-102,637,368 , GRCh38.p12 chr6: 102,150,369-102,189,493 LOC105377913
    nsv4385965copy number variation1nstd173human GRCh37 chr6: 152,355,874-152,393,650 , GRCh38.p12 chr6: 152,034,739-152,072,515 ESR1
    nsv4378041copy number variation1nstd173human GRCh37 chr6: 102,126,758-102,160,716 , GRCh38.p12 chr6: 101,678,883-101,712,841 GRIK2
    nsv4387039copy number variation1nstd173human GRCh37 chr6: 163,233,751-163,266,889 , GRCh38.p12 chr6: 162,812,719-162,845,857 PACRG
    nsv4379737copy number variation349nstd173human GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527 NME7
    nsv4369603copy number variation1nstd173human GRCh37 chr6: 101,919,536-101,944,941 , GRCh38.p12 chr6: 101,471,660-101,497,065 GRIK2
    nsv4384162copy number variation1nstd173human GRCh37 chr6: 102,018,509-102,043,717 , GRCh38.p12 chr6: 101,570,634-101,595,842 GRIK2
    nsv4387727copy number variation1nstd173human GRCh37 chr6: 152,657,391-152,682,267 , GRCh38.p12 chr6: 152,336,256-152,361,132 SYNE1
    nsv4378038copy number variation35nstd173human GRCh37 chr3: 89,394,579-89,419,375 , GRCh38.p12 chr3: 89,345,429-89,370,225 EPHA3
    nsv4376476copy number variation1nstd173human GRCh37 chr6: 152,877,565-152,900,568 , GRCh38.p12 chr6: 152,556,430-152,579,433 SYNE1
    nsv4381466copy number variation1nstd173human GRCh37 chr2: 34,787,577-34,839,181 , GRCh38.p12 chr2: 34,562,510-34,614,114 LOC105374459
    nsv4367783copy number variation1nstd173human GRCh37 chr4: 145,863,901-145,905,173 , GRCh38.p12 chr4: 144,942,749-144,984,021 ANAPC10
    nsv4366274copy number variation133nstd173human GRCh37 chr7: 75,354,113-75,375,909 , GRCh38.p12 chr7: 75,724,795-75,746,591 HIP1
    nsv4367022copy number variation1nstd173human GRCh37 chr4: 142,045,161-142,066,603 , GRCh38.p12 chr4: 141,124,007-141,145,449 RNF150
    nsv4375073copy number variation1nstd173human GRCh37 chr6: 125,227,741-125,248,671 , GRCh38.p12 chr6: 124,906,595-124,927,525 RNF217-AS1
    nsv4382377copy number variation1nstd173human GRCh37 chr6: 162,897,667-163,120,089 , GRCh38.p12 chr6: 162,476,635-162,699,057 PRKN, KRT8P44
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center