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 112

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5679102mobile element insertion1nstd211human GRCh38 chr5: 140,688,398-140,688,398 , GRCh37.p13 chr5: 140,067,983-140,067,983 HARS1
    nsv5633423insertion1nstd207human GRCh38 chr5: 140,685,994-140,685,994 , GRCh37.p13 chr5: 140,065,579-140,065,579 HARS1
    nsv5405830mobile element insertion1nstd206human GRCh38 chr5: 140,688,384-140,688,384 , GRCh37.p13 chr5: 140,067,969-140,067,969 HARS1
    nsv5381613copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,052,489-140,072,312 , GRCh38.p12 chr5: 140,672,904-140,692,727 WDR55, DND1, 2 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
    nsv5090927mobile element insertion1nstd203human GRCh38 chr5: 140,688,384-140,688,398 , GRCh37.p13 chr5: 140,067,969-140,067,983 HARS1
    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
    nsv4945149copy number variation1nstd200human GRCh38 chr5: 140,678,620-140,684,220 , GRCh37.p13 chr5: 140,058,205-140,063,805 HARS1
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805868copy number variation1nstd200human GRCh37 chr5: 140,058,163-140,063,833 , GRCh38.p12 chr5: 140,678,578-140,684,248 HARS1
    nsv4769359copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,060,429-140,070,831 , GRCh38.p12 chr5: 140,680,844-140,691,246 HARS1, HARS2
    nsv4681609copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,058,587-140,062,804 , GRCh38.p12 chr5: 140,679,002-140,683,219 HARS1
    nsv4597772copy number variation1nstd183human GRCh37 chr5: 140,052,935-140,052,989 , GRCh38.p12 chr5: 140,673,350-140,673,404 WDR55, HARS1, 1 more genes
    nsv4479257mobile element insertion1nstd166human GRCh37.p13 chr5: 140,067,969-140,067,969 , GRCh38.p12 chr5: 140,688,384-140,688,384 HARS1
    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
    nsv4394374copy number variation1nstd174human GRCh37 chr5: 140,050,382-140,053,590 , GRCh38.p12 chr5: 140,670,797-140,674,005 WDR55, DND1, 1 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
    nsv3924309copy number variation1nstd102humanPathogenic GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065 FCHSD1, LOC105378208, 183 more genes
    nsv3923450copy number variation1nstd102humanPathogenic GRCh37 chr5: 137,172,371-140,075,946 , NCBI36 chr5: 137,200,270-140,056,130 , GRCh38 chr5: 137,836,682-140,696,361 RNU6-236P, FAM13B, 89 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