U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 33

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3921211copy number variation1nstd102humanBenign GRCh38 chr3: 30,634,639-30,638,613 , GRCh37 chr3: 30,676,131-30,680,105 , NCBI36 chr3: 30,651,135-30,655,109 TGFBR2
    nsv3924423delins1nstd102humanLikely benign GRCh37 chr3: 30,691,969-30,691,999 , GRCh38 chr3: 30,650,477-30,650,507 TGFBR2
    nsv3918823copy number variation1nstd102humanUncertain significance GRCh38 chr3: 30,623,003-30,666,517 , NCBI36 chr3: 30,639,499-30,683,013 , GRCh37 chr3: 30,664,495-30,708,009 TGFBR2
    nsv3918783copy number variation1nstd102humanUncertain significance GRCh38 chr3: 30,628,928-30,656,356 , NCBI36 chr3: 30,645,424-30,672,852 , GRCh37 chr3: 30,670,420-30,697,848 TGFBR2
    nsv3919438copy number variation1nstd102humanUncertain significance NCBI36 chr3: 30,655,109-30,672,852 , GRCh37 chr3: 30,680,105-30,697,848 , GRCh38 chr3: 30,638,613-30,656,356 TGFBR2
    nsv4453846copy number variation2nstd102humanUncertain significance GRCh37 chr3: 30,684,776-30,698,392 , GRCh38.p12 chr3: 30,643,284-30,656,900 TGFBR2
    nsv5381418copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,732,902-30,735,937 , GRCh38.p12 chr3: 30,691,410-30,694,445 TGFBR2
    nsv7096711copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,732,892-30,733,091 , GRCh38.p12 chr3: 30,691,400-30,691,599 TGFBR2
    nsv7096710copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,729,856-30,730,023 , GRCh38.p12 chr3: 30,688,364-30,688,531 TGFBR2
    nsv5564343copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,729,866-30,730,013 , GRCh38.p12 chr3: 30,688,374-30,688,521 TGFBR2
    nsv6314935copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,729,876-30,730,003 , GRCh38.p12 chr3: 30,688,384-30,688,511 TGFBR2
    nsv3914314copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,664,495-30,697,848 , NCBI36 chr3: 30,639,499-30,672,852 , GRCh38 chr3: 30,623,003-30,656,356 TGFBR2
    nsv7096459copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,713,110-30,715,758 , GRCh38.p12 chr3: 30,671,618-30,674,266 TGFBR2
    nsv7136953copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,732,896-30,732,897 , GRCh38 chr3: 30,691,404-30,691,405 TGFBR2
    nsv7098728copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,648,061-30,648,353 , GRCh38 chr3: 30,606,569-30,606,861 TGFBR2, LOC105377015
    nsv6290128copy number variation1nstd102humanUncertain significance GRCh37 chr3: 30,648,060-30,648,117 , GRCh38 chr3: 30,606,568-30,606,625 TGFBR2, LOC105377015
    nsv3920506copy number variation1nstd102humanUncertain significance GRCh38 chr3: 30,638,613-30,754,170 , NCBI36 chr3: 30,655,109-30,770,666 , GRCh37 chr3: 30,680,105-30,795,662 TGFBR2, GADL1
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 TGFBR2, LOC102724104, 291 more genes
    nsv3913369copy number variation1nstd102humanPathogenic NCBI36 chr3: 29,206,432-35,025,542 , GRCh37.p13 chr3: 29,231,428-35,050,538 , GRCh38.p12 chr3: 29,189,937-35,009,046 TGFBR2, MTND4LP9, 61 more genes
    nsv3882929copy number variation1nstd102humanPathogenic GRCh37 chr3: 29,689,082-34,233,218 , GRCh38.p12 chr3: 29,647,591-34,191,726 TGFBR2, MIR548AY, 56 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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