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 369

    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
    nsv6737860copy number variation1nstd229human GRCh38 chr3: 194,633,684-194,643,434 , GRCh37.p13 chr3: 194,354,413-194,364,163 LSG1, TMEM44
    nsv6737551copy number variation1nstd229human GRCh38 chr3: 194,665,458-194,831,295 , GRCh37.p13 chr3: 194,386,187-194,552,024 FAM151AP1, LSG1, 4 more genes
    nsv6737508copy number variation1nstd229human GRCh38 chr3: 194,643,020-194,650,833 , GRCh37.p13 chr3: 194,363,749-194,371,562 LSG1
    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
    nsv6730425copy number variation1nstd229human GRCh38 chr3: 194,660,791-194,675,053 , GRCh37.p13 chr3: 194,381,520-194,395,782 LSG1
    nsv6729936copy number variation1nstd229human GRCh38 chr3: 194,595,632-194,782,335 , GRCh37.p13 chr3: 194,316,361-194,503,064 LINC01968, FAM43A, 6 more genes
    nsv6727494copy number variation1nstd229human GRCh38 chr3: 194,641,880-194,641,963 , GRCh37.p13 chr3: 194,362,609-194,362,692 LSG1
    nsv6723830copy number variation1nstd229human GRCh38 chr3: 194,665,636-194,990,341 , GRCh37.p13 chr3: 194,386,365-194,711,070 LOC105374292, LSG1, 6 more genes
    nsv6722403copy number variation1nstd229human GRCh38 chr3: 194,638,632-194,642,241 , GRCh37.p13 chr3: 194,359,361-194,362,970 LSG1
    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
    nsv6628936copy number variation1nstd224human GRCh37 chr3: 194,362,826-194,769,114 , GRCh38.p12 chr3: 194,642,097-195,048,385 LSG1, FAM43A, 7 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
    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
    nsv6278181insertion1nstd214human GRCh38 chr3: 194,663,763-194,663,763 , GRCh37.p13 chr3: 194,384,492-194,384,492 LSG1
    nsv6263284copy number variation1nstd214human GRCh38 chr3: 194,645,503-194,645,574 , GRCh37.p13 chr3: 194,366,232-194,366,303 LSG1
    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