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 264

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6736805copy number variation1nstd229human GRCh38 chr4: 55,554,546-55,558,337 , GRCh37.p13 chr4: 56,420,713-56,424,504 PDCL2
    nsv6733204copy number variation1nstd229human GRCh38 chr4: 55,557,096-55,562,563 , GRCh37.p13 chr4: 56,423,263-56,428,730 PDCL2
    nsv6731076copy number variation1nstd229human GRCh38 chr4: 55,562,102-55,566,477 , GRCh37.p13 chr4: 56,428,269-56,432,644 PDCL2
    nsv6725591copy number variation1nstd229human GRCh38 chr4: 55,515,301-55,598,400 , GRCh37.p13 chr4: 56,381,468-56,464,567 CLOCK, RN7SKP30, 2 more genes
    nsv6723357copy number variation1nstd229human GRCh38 chr4: 55,591,407-55,595,750 , GRCh37.p13 chr4: 56,457,574-56,461,917 NMU, PDCL2
    nsv6722401copy number variation1nstd229human GRCh38 chr4: 55,556,580-55,828,542 , GRCh37.p13 chr4: 56,422,747-56,694,708 EXOC1L, LOC105377661, 4 more genes
    nsv6720279copy number variation1nstd229human GRCh38 chr4: 55,564,862-55,964,774 , GRCh37.p13 chr4: 56,431,029-56,830,940 EXOC1, NMU, 8 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6573211inversion1nstd223human GRCh38 chr4: 55,556,553-55,557,960 , GRCh37.p13 chr4: 56,422,720-56,424,127 PDCL2
    nsv6564209inversion1nstd223human GRCh38 chr4: 55,588,889-55,589,946 , GRCh37.p13 chr4: 56,455,056-56,456,113 PDCL2
    nsv6395526copy number variation1nstd223human GRCh38 chr4: 55,591,407-55,595,745 , GRCh37.p13 chr4: 56,457,574-56,461,912 PDCL2, NMU
    nsv6390334copy number variation1nstd223human GRCh38 chr4: 55,560,737-55,561,023 , GRCh37.p13 chr4: 56,426,904-56,427,190 PDCL2
    nsv6389091copy number variation1nstd223human GRCh38 chr4: 55,577,998-55,580,535 , GRCh37.p13 chr4: 56,444,165-56,446,702 PDCL2
    nsv6382024copy number variation1nstd223human GRCh38 chr4: 55,554,546-55,558,333 , GRCh37.p13 chr4: 56,420,713-56,424,500 PDCL2
    nsv6315421copy number variation1nstd102humanPathogenic GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280 METTL5P3, RPL38P3, 38 more genes
    nsv6311837copy number variation2nstd102humanUncertain significance GRCh37 chr4: 55,124,936-57,798,318 , GRCh38.p12 chr4: 54,258,769-56,932,152 GLDCP1, KDR, 54 more genes
    nsv6299429copy number variation1nstd186human GRCh37 chr4: 56,432,055-56,432,112 , GRCh38.p12 chr4: 55,565,888-55,565,945 PDCL2
    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