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 182

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097141copy number variation1nstd102humanUncertain significance GRCh37 chr5: 36,195,246-36,241,900 , GRCh38.p12 chr5: 36,195,144-36,241,798 NADK2
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv6772343copy number variation1nstd229human GRCh38 chr5: 36,201,745-36,202,108 , GRCh37.p13 chr5: 36,201,847-36,202,210 NADK2
    nsv6770994copy number variation1nstd229human GRCh38 chr5: 36,215,312-36,275,708 , GRCh37.p13 chr5: 36,215,414-36,275,810 NADK2, RANBP3L
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6768286copy number variation1nstd229human GRCh38 chr5: 36,234,589-36,237,895 , GRCh37.p13 chr5: 36,234,691-36,237,997 NADK2
    nsv6762217copy number variation1nstd229human GRCh38 chr5: 36,239,665-36,245,897 , GRCh37.p13 chr5: 36,239,767-36,245,999 NADK2, RANBP3L
    nsv6758744copy number variation1nstd229human GRCh38 chr5: 36,195,001-36,197,900 , GRCh37.p13 chr5: 36,195,103-36,198,002 NADK2
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630401copy number variation1nstd224human GRCh37 chr5: 36,195,350-36,324,582 , GRCh38.p12 chr5: 36,195,248-36,324,480 NADK2, RANBP3L
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6386490copy number variation1nstd223human GRCh38 chr5: 36,216,301-36,217,500 , GRCh37.p13 chr5: 36,216,403-36,217,602 NADK2
    nsv6384468copy number variation1nstd223human GRCh38 chr5: 36,203,757-36,205,644 , GRCh37.p13 chr5: 36,203,859-36,205,746 NADK2
    nsv6380024copy number variation1nstd223human GRCh38 chr5: 36,202,676-36,318,884 , GRCh37.p13 chr5: 36,202,778-36,318,986 NADK2, RANBP3L
    nsv6377422copy number variation1nstd223human GRCh38 chr5: 36,206,932-36,207,577 , GRCh37.p13 chr5: 36,207,034-36,207,679 NADK2
    nsv6376780copy number variation1nstd223human GRCh38 chr5: 36,195,732-36,196,433 , GRCh37.p13 chr5: 36,195,834-36,196,535 NADK2
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6312197copy number variation1nstd102humanUncertain significance GRCh37 chr5: 36,206,097-36,207,258 , GRCh38.p12 chr5: 36,205,995-36,207,156 NADK2
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 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