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 96

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097512copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,930,285-140,078,137 , GRCh38.p12 chr5: 140,550,700-140,698,552 TMCO6, ZMAT2, 15 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 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
    nsv7043618inversion1nstd229human GRCh38 chr5: 140,515,390-140,897,647 , GRCh37.p13 chr5: 139,894,975-140,144,409 PCDHA1, TMCO6, 39 more genes
    nsv6562823inversion1nstd223human GRCh38 chr5: 140,515,380-140,897,647 , GRCh37.p13 chr5: 139,894,965-140,144,409 HARS2, ANKHD1, 39 more genes
    nsv6408594copy number variation1nstd223human GRCh38 chr5: 140,515,601-140,836,000 , GRCh37.p13 chr5: 139,895,186-140,144,409 PCDHA2, RPL36P11, 31 more genes
    nsv6407401copy number variation1nstd223human GRCh38 chr5: 140,339,301-140,944,600 , GRCh37.p13 chr5: 139,718,886-140,144,409 IK, RNU4-14P, 43 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
    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
    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
    nsv5222563copy number variation1nstd204human GRCh37.p13 chr5: 139,926,986-139,957,885 , GRCh38.p13 chr5: 140,547,401-140,578,300 EIF4EBP3, SRA1, 5 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4455072copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,447,779-140,047,037 , GRCh38.p12 chr5: 140,068,194-140,667,452 LOC112267855, RNU4-14P, 23 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv4127817copy number variation1nstd166human GRCh37.p13 chr5: 139,935,000-139,945,000 , GRCh38.p12 chr5: 140,555,415-140,565,415 APBB3, SRA1, 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