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 106

    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
    nsv7048655inversion1nstd229human GRCh38 chr5: 140,924,725-141,060,299 , GRCh37.p13 chr5: 140,304,310-140,439,884 , GRCh37.p13 chr5|NW_004775428.1: 159,901-295,475 PCDHAC2, PCDHA8, 18 more genes
    nsv6797370copy number variation1nstd229human GRCh38 chr5: 141,030,461-141,053,860 , GRCh37.p13 chr5|NW_004775428.1: 265,637-289,036 , GRCh37.p13 chr5: 140,410,046-140,433,445 PCDHB1-AS1, PCDHB1, 1 more genes
    nsv6778533copy number variation1nstd229human GRCh38 chr5: 141,012,001-141,086,400 , GRCh37.p13 chr5|NW_004775428.1: 247,177-321,576 , GRCh37.p13 chr5: 140,391,586-140,465,983 PCDHA9, PCDHA11, 18 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
    nsv6568332inversion1nstd223human GRCh37.p13 chr5|NW_004775428.1: 292,104-292,427 , GRCh38 chr5: 141,056,928-141,057,251 , GRCh37.p13 chr5: 140,436,513-140,436,836 PCDHB1, PCDHB@, 1 more genes
    nsv6561574inversion1nstd223human GRCh37.p13 chr5|NW_004775428.1: 289,887-290,639 , GRCh38 chr5: 141,054,711-141,055,463 , GRCh37.p13 chr5: 140,434,296-140,435,048 PCDHB1, PCDHB@, 1 more genes
    nsv6414972copy number variation1nstd223human GRCh38 chr5: 140,949,872-141,050,529 , GRCh37.p13 chr5|NW_004775428.1: 185,048-285,705 , GRCh37.p13 chr5: 140,329,457-140,430,114 PCDHB1-AS1, PCDHACT, 18 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
    nsv6406042copy number variation1nstd223human GRCh38 chr5: 141,030,461-141,053,855 , GRCh37.p13 chr5|NW_004775428.1: 265,637-289,031 , GRCh37.p13 chr5: 140,410,046-140,433,440 PCDHB1, PCDHB@, 1 more genes
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6403869copy number variation1nstd223human GRCh38 chr5: 141,059,401-141,554,400 , GRCh37.p13 chr5: 140,438,986-140,687,716 , GRCh37.p13 chr5|NW_004775428.1: 294,577-543,325 PCDHG@, PCDHGC4, 50 more genes
    nsv6290261copy number variation1nstd102humanPathogenic GRCh37 chr5: 139,493,717-140,517,454 , GRCh38.p12 chr5: 140,114,132-141,137,872 PCDHA2, RPL36P11, 57 more genes
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135117copy number variation1nstd213human GRCh37 chr5: 140,060,000-141,240,001 , GRCh38.p12 chr5: 140,680,415-141,860,436 DIAPH1, HARS1, 85 more genes
    nsv5467391copy number variation1nstd206human GRCh37.p13 chr5|NW_004775428.1: 287,076-287,140 , GRCh38 chr5: 141,051,900-141,051,964 , GRCh37.p13 chr5: 140,431,485-140,431,549 PCDHB@, PCDHB1-AS1, 1 more genes
    nsv5466798copy number variation1nstd206human GRCh37.p13 chr5|NW_004775428.1: 294,767-294,930 , GRCh38 chr5: 141,059,591-141,059,754 , GRCh37.p13 chr5: 140,439,176-140,439,339 PCDHB@, PCDHB1-AS1, 1 more genes
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 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