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 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6752891copy number variation1nstd229human GRCh38 chr4: 164,167,222-164,258,455 , GRCh37.p13 chr4: 165,088,374-165,179,607 MARCHF1, LOC100288073, 1 more genes
    nsv6751864copy number variation1nstd229human GRCh38 chr4: 164,039,828-165,202,299 , GRCh37.p13 chr4: 164,960,980-166,123,451 LOC391711, TRIM75, 21 more genes
    nsv6749310copy number variation1nstd229human GRCh38 chr4: 164,179,456-164,220,911 , GRCh37.p13 chr4: 165,100,608-165,142,063 LOC100288073, ANP32CP, 1 more genes
    nsv6746908copy number variation1nstd229human GRCh38 chr4: 164,174,017-164,427,565 , GRCh37.p13 chr4: 165,095,169-165,348,717 MARCHF1, LOC100288073, 1 more genes
    nsv6746282copy number variation1nstd229human GRCh38 chr4: 164,150,106-164,641,964 , GRCh37.p13 chr4: 165,071,258-165,563,116 RNU6-284P, MARCHF1, 2 more genes
    nsv6745157copy number variation1nstd229human GRCh38 chr4: 164,197,446-164,197,544 , GRCh37.p13 chr4: 165,118,598-165,118,696 ANP32CP, MARCHF1
    nsv6740482copy number variation1nstd229human GRCh38 chr4: 164,057,383-165,303,005 , GRCh37.p13 chr4: 164,978,535-166,224,157 TRIM60P14, LOC391711, 24 more genes
    nsv6738203copy number variation1nstd229human GRCh38 chr4: 164,164,217-164,305,307 , GRCh37.p13 chr4: 165,085,369-165,226,459 LOC100288073, ANP32CP, 1 more genes
    nsv6636463copy number variation1nstd102humanUncertain significance GRCh37 chr4: 165,018,011-165,278,347 , GRCh38.p12 chr4: 164,096,859-164,357,195 ANP32CP, LOC100288073, 1 more genes
    nsv6636318copy number variation1nstd102humanUncertain significance GRCh37 chr4: 161,461,677-166,911,259 , GRCh38.p12 chr4: 160,540,525-165,990,107 LOC107986325, NACA3P, 60 more genes
    nsv6636254copy number variation1nstd102humanUncertain significance GRCh37 chr4: 164,980,534-166,223,066 , GRCh38.p12 chr4: 164,059,382-165,301,914 ANP32CP, GK3, 24 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629625copy number variation1nstd224human GRCh37 chr4: 165,013,637-165,168,921 , GRCh38.p12 chr4: 164,092,485-164,247,769 ANP32CP, MARCHF1, 1 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
    nsv6134917copy number variation1nstd213human GRCh37 chr4: 163,890,000-165,780,001 , GRCh38.p12 chr4: 162,968,848-164,858,849 NPY1R, NPY5R, 18 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 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