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 336

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056404inversion1nstd229human GRCh38 chr7: 45,643,008-53,582,757 , GRCh37.p13 chr7: 45,682,607-53,650,450 PKD1L1, FIGNL1, 79 more genes
    nsv7056210inversion1nstd229human GRCh38 chr7: 45,705,342-45,705,405 , GRCh37.p13 chr7: 45,744,941-45,745,004 ADCY1
    nsv7049893inversion1nstd229human GRCh38 chr7: 45,597,910-45,605,630 , GRCh37.p13 chr7: 45,637,509-45,645,229 ADCY1
    nsv7046943inversion1nstd229human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 CDC14C, ROBO2P1, 79 more genes
    nsv6836157copy number variation1nstd229human GRCh38 chr7: 45,601,996-45,609,846 , GRCh37.p13 chr7: 45,641,595-45,649,445 ADCY1
    nsv6834800copy number variation1nstd229human GRCh38 chr7: 45,695,413-45,695,877 , GRCh37.p13 chr7: 45,735,012-45,735,476 ADCY1
    nsv6832571copy number variation1nstd229human GRCh38 chr7: 45,713,932-45,716,140 , GRCh37.p13 chr7: 45,753,531-45,755,739 ADCY1
    nsv6831782copy number variation1nstd229human GRCh38 chr7: 45,676,953-45,677,059 , GRCh37.p13 chr7: 45,716,552-45,716,658 ADCY1
    nsv6829387copy number variation1nstd229human GRCh38 chr7: 45,655,703-45,655,784 , GRCh37.p13 chr7: 45,695,302-45,695,383 ADCY1
    nsv6829165copy number variation1nstd229human GRCh38 chr7: 45,625,415-45,629,872 , GRCh37.p13 chr7: 45,665,014-45,669,471 ADCY1
    nsv6827269copy number variation1nstd229human GRCh38 chr7: 45,599,016-45,602,498 , GRCh37.p13 chr7: 45,638,615-45,642,097 ADCY1
    nsv6821594copy number variation1nstd229human GRCh38 chr7: 45,629,574-45,636,822 , GRCh37.p13 chr7: 45,669,173-45,676,421 ADCY1
    nsv6821260copy number variation1nstd229human GRCh38 chr7: 45,685,429-45,685,506 , GRCh37.p13 chr7: 45,725,028-45,725,105 ADCY1
    nsv6818177copy number variation1nstd229human GRCh38 chr7: 45,632,516-45,632,551 , GRCh37.p13 chr7: 45,672,115-45,672,150 ADCY1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6614285copy number variation1nstd223human GRCh38 chr7: 45,697,264-45,697,640 , GRCh37.p13 chr7: 45,736,863-45,737,239 ADCY1
    nsv6611707copy number variation1nstd223human GRCh38 chr7: 45,610,762-45,611,112 , GRCh37.p13 chr7: 45,650,361-45,650,711 ADCY1
    nsv6607880copy number variation1nstd223human GRCh38 chr7: 45,593,114-45,594,748 , GRCh37.p13 chr7: 45,632,713-45,634,347 ADCY1
    nsv6606211copy number variation1nstd223human GRCh38 chr7: 45,598,801-45,602,600 , GRCh37.p13 chr7: 45,638,400-45,642,199 ADCY1
    nsv6602019copy number variation1nstd223human GRCh38 chr7: 45,662,784-45,663,363 , GRCh37.p13 chr7: 45,702,383-45,702,962 ADCY1
    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