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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148072copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 193,343,827-194,599,635 , GRCh38.p12 chr3: 193,626,038-194,878,906 CPN2, GP5, 36 more genes
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv6732659copy number variation1nstd229human GRCh38 chr3: 194,391,019-194,558,345 , GRCh37.p13 chr3: 194,111,748-194,279,074 ATP13A3, ATP13A3-DT, 2 more genes
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6727962copy number variation1nstd229human GRCh38 chr3: 194,215,451-194,451,362 , GRCh37.p13 chr3: 193,933,240-194,172,091 LRRC15, LINC02036, 6 more genes
    nsv6727467copy number variation1nstd229human GRCh38 chr3: 194,397,482-194,440,381 , GRCh37.p13 chr3: 194,118,211-194,161,110 GP5, ATP13A3
    nsv6718222copy number variation1nstd229human GRCh38 chr3: 194,179,860-194,436,927 , GRCh37.p13 chr3: 193,897,649-194,157,656 GP5, LINC02048, 6 more genes
    nsv6636634copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,396,762-195,009,038 , GRCh38.p12 chr3: 193,678,973-195,288,309 LINC02036, LINC02026, 45 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628551copy number variation1nstd224human GRCh37 chr3: 193,855,650-194,188,614 , GRCh38.p12 chr3: 194,137,861-194,467,885 LINC02036, LOC107986172, 9 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6313865copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,836,939-194,169,926 , GRCh38.p12 chr3: 194,119,150-194,449,197 ATP13A3, CPN2, 10 more genes
    nsv6313527copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,607,378-194,745,252 , GRCh38.p12 chr3: 192,889,589-195,024,523 LINC02036, HES1, 48 more genes
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 LINC01972, LINC02026, 174 more genes
    nsv6290248copy number variation1nstd102humanPathogenic GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300 PIGZ, LOC107986173, 156 more genes
    nsv6135007copy number variation1nstd213human GRCh37 chr3: 194,040,000-194,250,001 , GRCh38.p12 chr3: 194,322,211-194,529,272 CPN2, GP5, 3 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv4928324copy number variation1nstd200human GRCh38 chr3: 194,384,080-194,397,129 , GRCh37.p13 chr3: 194,104,809-194,117,858 GP5
    nsv4925015copy number variation1nstd200human GRCh38 chr3: 194,179,860-194,436,927 , GRCh37.p13 chr3: 193,897,649-194,157,656 CPN2, LINC00887, 6 more genes
    nsv4596324copy number variation1nstd183human GRCh37 chr3: 193,962,049-194,571,078 , GRCh38.p12 chr3: 194,244,260-194,850,349 , LINC01968, 20 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