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 473

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144715insertion1nstd232human GRCh37.p13 chr5: 140,862,322-140,862,322 , GRCh38.p12 chr5: 141,482,755-141,482,755 PCDHGB3, PCDHGA11, 19 more genes
    nsv7057161inversion1nstd229human GRCh38 chr5: 141,377,317-141,379,850 , GRCh37.p13 chr5: 140,756,884-140,759,417 PCDHGB1, PCDHGA5, 8 more genes
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv7055899inversion1nstd229human GRCh38 chr5: 141,375,483-141,377,554 , GRCh37.p13 chr5: 140,755,050-140,757,121 PCDHGA1, PCDHGA4, 8 more genes
    nsv7055264inversion1nstd229human GRCh38 chr5: 141,397,100-141,397,151 , GRCh37.p13 chr5: 140,776,667-140,776,718 PCDHGB5, PCDHGB1, 12 more genes
    nsv6797907copy number variation1nstd229human GRCh38 chr5: 141,378,268-141,382,142 , GRCh37.p13 chr5: 140,757,835-140,761,709 PCDHGB2, PCDHGA4, 9 more genes
    nsv6795088copy number variation1nstd229human GRCh38 chr5: 141,480,314-141,482,754 , GRCh37.p13 chr5: 140,859,881-140,862,321 PCDHGA8, PCDHGA1, 19 more genes
    nsv6793509copy number variation1nstd229human GRCh38 chr5: 141,510,901-141,517,000 , GRCh37.p13 chr5: 140,890,468-140,896,567 PCDHGA1, PCDHGA7, 22 more genes
    nsv6790325copy number variation1nstd229human GRCh38 chr5: 141,511,568-141,511,774 , GRCh37.p13 chr5: 140,891,135-140,891,341 PCDHGB6, PCDHGB2, 21 more genes
    nsv6788179copy number variation1nstd229human GRCh38 chr5: 141,421,704-141,425,746 , GRCh37.p13 chr5: 140,801,271-140,805,313 PCDHGB4, PCDHG@, 18 more genes
    nsv6786654copy number variation1nstd229human GRCh38 chr5: 141,430,970-141,436,047 , GRCh37.p13 chr5: 140,810,537-140,815,614 PCDHGA1, PCDHGA8, 18 more genes
    nsv6786281copy number variation1nstd229human GRCh38 chr5: 141,505,481-141,510,945 , GRCh37.p13 chr5: 140,885,048-140,890,512 PCDHGA11, PCDHGB3, 21 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
    nsv6785857copy number variation1nstd229human GRCh38 chr5: 141,495,087-141,497,917 , GRCh37.p13 chr5: 140,874,654-140,877,484 PCDHGA10, PCDHGC4, 21 more genes
    nsv6778548copy number variation1nstd229human GRCh38 chr5: 141,387,501-141,398,200 , GRCh37.p13 chr5: 140,767,068-140,777,767 PCDHGB1, PCDHGA4, 12 more genes
    nsv6778130copy number variation1nstd229human GRCh38 chr5: 141,485,723-141,486,291 , GRCh37.p13 chr5: 140,865,290-140,865,858 PCDHGA9, PCDHGA2, 20 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
    nsv6636181copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 140,865,418-140,865,497 , GRCh38 chr5: 141,485,851-141,485,930 PCDHGC3, PCDHGB4, 20 more genes
    nsv6572268inversion1nstd223human GRCh38 chr5: 141,456,104-141,456,705 , GRCh37.p13 chr5: 140,835,671-140,836,272 PCDHGB2, PCDHGB6, 18 more genes
    nsv6565965inversion1nstd223human GRCh38 chr5: 141,375,482-141,377,554 , GRCh37.p13 chr5: 140,755,049-140,757,121 PCDHGA2, PCDHGA5, 8 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