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 312

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097763copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,252,617-94,252,729 , GRCh38.p12 chr7: 94,623,305-94,623,417 SGCE, CASD1
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv7043317inversion1nstd229human GRCh38 chr7: 94,629,510-94,629,529 , GRCh37.p13 chr7: 94,258,822-94,258,841 CASD1, SGCE
    nsv6837036copy number variation1nstd229human GRCh38 chr7: 94,420,155-94,527,294 , GRCh37.p13 chr7: 94,049,467-94,156,606 LOC105375404, CASD1, 2 more genes
    nsv6836765copy number variation1nstd229human GRCh38 chr7: 94,408,736-94,525,792 , GRCh37.p13 chr7: 94,038,048-94,155,104 LOC105375404, CASD1, 2 more genes
    nsv6830899copy number variation1nstd229human GRCh38 chr7: 94,567,101-94,580,000 , GRCh37.p13 chr7: 94,196,413-94,209,312 CASD1
    nsv6827739copy number variation1nstd229human GRCh38 chr7: 94,563,379-94,566,410 , GRCh37.p13 chr7: 94,192,691-94,195,722 CASD1
    nsv6825987copy number variation1nstd229human GRCh38 chr7: 94,604,817-94,608,434 , GRCh37.p13 chr7: 94,234,129-94,237,746 SGCE, CASD1
    nsv6819203copy number variation1nstd229human GRCh38 chr7: 94,524,301-94,528,200 , GRCh37.p13 chr7: 94,153,613-94,157,512 CASD1, LOC105375404
    nsv6818655copy number variation1nstd229human GRCh38 chr7: 94,561,504-94,632,741 , GRCh37.p13 chr7: 94,190,816-94,262,053 CASD1, SGCE
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 more genes
    nsv6634640copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,252,695-94,252,791 , GRCh38 chr7: 94,623,383-94,623,479 SGCE, CASD1
    nsv6634607copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,232,052-94,238,873 , GRCh38 chr7: 94,602,740-94,609,561 SGCE, CASD1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632408copy number variation1nstd224human GRCh37 chr7: 94,027,699-94,141,226 , GRCh38.p12 chr7: 94,398,387-94,511,914 RNU6-1328P, LOC105375404, 2 more genes
    nsv6619078copy number variation1nstd223human GRCh38 chr7: 94,546,201-94,547,100 , GRCh37.p13 chr7: 94,175,513-94,176,412 CASD1, LOC105375404
    nsv6618440copy number variation1nstd223human GRCh38 chr7: 94,551,001-94,552,100 , GRCh37.p13 chr7: 94,180,313-94,181,412 LOC105375404, CASD1
    nsv6616700copy number variation1nstd223human GRCh38 chr7: 94,569,843-94,570,526 , GRCh37.p13 chr7: 94,199,155-94,199,838 CASD1
    nsv6614291copy number variation1nstd223human GRCh38 chr7: 94,565,253-94,565,634 , GRCh37.p13 chr7: 94,194,565-94,194,946 CASD1
    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