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 90

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5457164copy number variation1nstd206human GRCh38 chr5: 85,531,389-85,777,329 , GRCh37.p13 chr5: 84,827,207-85,073,147 LOC645181, RPS2P25, 1 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4680515copy number variation1nstd189human GRCh37.p13 chr5: 84,125,705-86,325,929 , GRCh38.p12 chr5: 84,829,887-87,030,112 COX7C, NBPF22P, 17 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4457339copy number variation1nstd102humanPathogenic GRCh37 chr5: 83,497,559-88,416,354 , GRCh38.p12 chr5: 84,201,741-89,120,537 LINC02144, NBPF22P, 47 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
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv4129828copy number variation1nstd166human GRCh37.p13 chr5: 84,851,878-85,145,420 , GRCh38.p12 chr5: 85,556,060-85,849,602 LOC105379061, LOC105379062, 1 more genes
    nsv3924896copy number variation1nstd102humanPathogenic GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678 LOC107986438, GGCTP1, 254 more genes
    nsv3917856copy number variation1nstd102humanPathogenic GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153 CSNK1A1P3, POLR3G, 413 more genes
    nsv3917405copy number variation1nstd102humanPathogenic NCBI36 chr5: 85,081,381-89,338,394 , GRCh37.p13 chr5: 85,045,625-89,302,638 , GRCh38.p12 chr5: 85,749,807-90,006,821 LOC105379065, LOC105379062, 42 more genes
    nsv3914813copy number variation1nstd102humanBenign NCBI36 chr5: 84,805,976-85,496,267 , GRCh37 chr5: 84,770,220-85,460,511 , GRCh38 chr5: 85,474,402-86,164,693 LOC645181, PTP4A1P4, 4 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv2349786short tandem repeat9nstd128human GRCh37 chr5: 85,058,212-85,058,242 , GRCh38.p12 chr5: 85,762,394-85,762,424 RPS2P25
    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