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 141

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075760inversion1nstd229human GRCh38 chr19: 54,368,885-57,042,988 , GRCh37.p13 chr19: 55,595,687-57,554,356 ZSCAN5C, TMEM190, 137 more genes
    nsv7067331inversion1nstd229human GRCh38 chr19: 54,730,353-56,291,074 , GRCh37.p13 chr19: 55,595,687-56,802,443 NLRP2, KIR2DP1, 85 more genes
    nsv7063630inversion1nstd229human GRCh38 chr19: 54,312,295-55,433,689 , GRCh37.p13 chr19|NW_004166865.1: 286,662-1,058,686 BRSK1, VN1R104P, 69 more genes
    nsv7062087inversion1nstd229human GRCh38 chr19: 54,368,882-57,042,981 , GRCh37.p13 chr19: 55,595,687-57,554,349 BRSK1, ZIM2, 137 more genes
    nsv7060532inversion1nstd229human GRCh38 chr19: 54,888,784-55,573,986 , GRCh37.p13 chr19: 55,595,687-56,085,352 SSC5D, MIR6804, 41 more genes
    nsv7010190copy number variation1nstd229human GRCh38 chr19: 55,421,687-55,427,581 , GRCh37.p13 chr19: 55,933,054-55,938,948 SHISA7, LOC105372462
    nsv6998458copy number variation1nstd229human GRCh38 chr19: 55,266,101-55,489,000 , GRCh37.p13 chr19: 55,777,469-56,000,367 TMEM150B, BRSK1, 17 more genes
    nsv6637872copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,909,965-55,975,611 , GRCh38.p12 chr19: 55,398,597-55,464,244 RPL28, UBE2S, 4 more genes
    nsv6597417inversion1nstd223human GRCh38 chr19: 55,425,677-55,427,001 , GRCh37.p13 chr19: 55,937,044-55,938,368 LOC105372462, SHISA7
    nsv6596657inversion1nstd223human GRCh38 chr19: 54,888,785-55,573,993 , GRCh37.p13 chr19: 55,595,687-56,085,359 SBK2, BRSK1, 41 more genes
    nsv6529975copy number variation1nstd223human GRCh38 chr19: 55,307,661-55,545,550 , GRCh37.p13 chr19: 55,819,029-56,056,916 BRSK1, SBK2, 18 more genes
    nsv6515868copy number variation1nstd223human GRCh38 chr19: 55,430,888-55,431,510 , GRCh37.p13 chr19: 55,942,255-55,942,877 SHISA7
    nsv6315178copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,434,660-56,463,734 , GRCh38.p12 chr19: 54,923,292-55,952,368 RDH13, SSC5D, 62 more genes
    nsv6291483copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 55,247,893-56,503,347 , GRCh38.p12 chr19: 54,911,986-55,991,981 IL11, PTPRH, 62 more genes
    nsv6227489copy number variation1nstd214human GRCh38 chr19: 55,437,791-55,437,936 , GRCh37.p13 chr19: 55,949,158-55,949,303 SHISA7
    nsv6209061copy number variation1nstd214human GRCh38 chr19: 55,439,770-55,439,827 , GRCh37.p13 chr19: 55,951,137-55,951,194 SHISA7
    nsv6133475copy number variation1nstd213human GRCh37 chr19: 55,370,000-56,020,001 , GRCh38.p12 chr19: 54,911,986-55,508,634 IL11, PTPRH, 38 more genes
    nsv6055406copy number variation1nstd212human GRCh38 chr19: 55,437,948-55,438,017 , GRCh37.p13 chr19: 55,949,315-55,949,384 SHISA7
    nsv6054006copy number variation1nstd212human GRCh38 chr19: 55,434,598-55,434,679 , GRCh37.p13 chr19: 55,945,965-55,946,046 SHISA7
    nsv6047667copy number variation1nstd212human GRCh38 chr19: 55,434,309-55,434,376 , GRCh37.p13 chr19: 55,945,676-55,945,743 SHISA7
    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