U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 260

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6797577copy number variation1nstd229human GRCh38 chr5: 141,165,423-141,188,588 , GRCh37.p13 chr5|NW_004775428.1: 400,599-423,764 , GRCh37.p13 chr5: 140,545,004-140,568,161 PCDHB16, PCDHB7, 3 more genes
    nsv6797503copy number variation1nstd229human GRCh38 chr5: 141,119,601-141,269,700 , GRCh37.p13 chr5: 140,499,183-140,649,269 , GRCh37.p13 chr5|NW_004775428.1: 354,777-504,876 PCDHB14, PCDHB11, 17 more genes
    nsv6797457copy number variation1nstd229human GRCh38 chr5: 141,086,601-141,250,700 , GRCh37.p13 chr5|NW_004775428.1: 321,777-485,876 , GRCh37.p13 chr5: 140,466,184-140,630,268 PCDHB12, PCDHB15, 17 more genes
    nsv6792459copy number variation1nstd229human GRCh38 chr5: 141,183,913-141,186,482 , GRCh37.p13 chr5: 140,563,488-140,566,056 , GRCh37.p13 chr5|NW_004775428.1: 419,089-421,658 PCDHB16, PCDHB@, 1 more genes
    nsv6785934copy number variation1nstd229human GRCh38 chr5: 141,174,601-142,728,000 , GRCh37.p13 chr5: 140,687,717-142,107,565 TAF7, RNF14, 64 more genes
    nsv6636350copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,082,762-140,773,954 , GRCh38.p12 chr5: 140,703,177-141,394,387 PCDHA13, PCDHA10, 61 more genes
    nsv6630308copy number variation1nstd224human GRCh37 chr5: 140,553,581-140,573,366 , GRCh38.p12 chr5: 141,174,000-141,193,793 PCDHB@, PCDHB10, 4 more genes
    nsv6630113copy number variation1nstd224human GRCh37 chr5: 140,559,849-140,604,213 , GRCh38.p12 chr5: 141,180,268-141,224,641 PCDHB@, PCDHB14, 7 more genes
    nsv6630112copy number variation1nstd224human GRCh37 chr5: 140,554,769-140,590,766 , GRCh38.p12 chr5: 141,175,188-141,211,194 PCDHB@, PCDHB12, 6 more genes
    nsv6630059copy number variation1nstd224human GRCh37 chr5: 140,559,849-140,590,766 , GRCh38.p12 chr5: 141,180,268-141,211,194 PCDHB@, PCDHB12, 5 more genes
    nsv6630058copy number variation1nstd224human GRCh37 chr5: 140,559,849-140,573,366 , GRCh38.p12 chr5: 141,180,268-141,193,793 PCDHB@, PCDHB10, 3 more genes
    nsv6630057copy number variation1nstd224human GRCh37 chr5: 140,552,652-140,627,390 , GRCh38.p12 chr5: 141,173,071-141,247,822 PCDHB15, PCDHB8, 11 more genes
    nsv6415510copy number variation1nstd223human GRCh37.p13 chr5|NW_004775428.1: 413,921-450,010 , GRCh38 chr5: 141,178,745-141,214,834 , GRCh37.p13 chr5: 140,558,326-140,594,406 PCDHB13, PCDHB10, 6 more genes
    nsv6412323copy number variation1nstd223human GRCh38 chr5: 141,171,901-141,179,800 , GRCh37.p13 chr5|NW_004775428.1: 407,077-414,976 , GRCh37.p13 chr5: 140,551,482-140,559,381 PCDHB8, PCDHB16, 2 more genes
    nsv6409325copy number variation1nstd223human GRCh38 chr5: 141,184,442-141,189,010 , GRCh37.p13 chr5|NW_004775428.1: 419,618-424,186 , GRCh37.p13 chr5: 140,564,017-140,568,583 PCDHB@, PCDHB16, 1 more genes
    nsv6409059copy number variation1nstd223human GRCh37.p13 chr5|NW_004775428.1: 409,677-436,876 , GRCh38 chr5: 141,174,501-141,201,700 , GRCh37.p13 chr5: 140,554,082-140,581,273 PCDHB11, PCDHB8, 5 more genes
    nsv6408486copy number variation1nstd223human GRCh38 chr5: 141,050,901-141,250,300 , GRCh37.p13 chr5|NW_004775428.1: 286,077-485,476 , GRCh37.p13 chr5: 140,430,486-140,629,868 PCDHB@, PCDHB14, 19 more genes
    nsv6407876copy number variation1nstd223human GRCh37.p13 chr5|NW_004775428.1: 406,877-431,076 , GRCh38 chr5: 141,171,701-141,195,900 , GRCh37.p13 chr5: 140,551,282-140,575,473 PCDHB@, PCDHB7, 4 more genes
    nsv6407870copy number variation1nstd223human GRCh38 chr5: 141,175,501-141,181,000 , GRCh37.p13 chr5|NW_004775428.1: 410,677-416,176 , GRCh37.p13 chr5: 140,555,082-140,560,581 PCDHB7, PCDHB@, 2 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    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