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 73

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895082copy number variation1nstd102humanBenign GRCh37 chr16: 1,272,275-1,273,638 , GRCh38.p12 chr16: 1,222,275-1,223,638 TPSG1
    nsv3895003copy number variation1nstd102humanBenign GRCh37 chr16: 1,272,275-1,273,591 , GRCh38.p12 chr16: 1,222,275-1,223,591 TPSG1
    nsv3906835copy number variation1nstd102humanBenign GRCh37 chr16: 1,272,275-1,273,586 , GRCh38.p12 chr16: 1,222,275-1,223,586 TPSG1
    nsv3892464copy number variation1nstd102humanBenign GRCh37 chr16: 1,251,760-1,272,676 , GRCh38.p12 chr16: 1,201,760-1,222,676 TPSG1, CACNA1H
    nsv6309835copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,244,952-1,270,994 , GRCh38.p12 chr16: 1,194,952-1,220,994 TPSG1, CACNA1H
    nsv5564224copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,244,962-1,270,994 , GRCh38.p12 chr16: 1,194,962-1,220,994 TPSG1, CACNA1H
    nsv7093306copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,270,644-1,270,820 , GRCh38 chr16: 1,220,644-1,220,820 TPSG1, CACNA1H
    nsv4682712copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,244,952-1,271,014 , GRCh38.p12 chr16: 1,194,952-1,221,014 TPSG1, CACNA1H
    nsv7094646copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,248,595-1,270,994 , GRCh38.p12 chr16: 1,198,595-1,220,994 TPSG1, CACNA1H
    nsv5380991copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,248,605-1,270,994 , GRCh38.p12 chr16: 1,198,605-1,220,994 TPSG1, CACNA1H
    nsv4682403copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,264,952-1,271,014 , GRCh38.p12 chr16: 1,214,952-1,221,014 TPSG1, CACNA1H
    nsv6309836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,264,952-1,270,994 , GRCh38.p12 chr16: 1,214,952-1,220,994 TPSG1, CACNA1H
    nsv3907544copy number variation1nstd102humanBenign GRCh37 chr16: 1,261,282-1,288,881 , GRCh38.p12 chr16: 1,211,282-1,238,880 TPSG1, TPSB2, 2 more genes
    nsv4455594copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327 TPSG1, JPT2, 128 more genes
    nsv3919589copy number variation1nstd102humanPathogenic NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582 TPSG1, C1QTNF8, 127 more genes
    nsv3914731copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,722-1,867,327 , NCBI36 chr16: 36,722-1,857,329 , GRCh37 chr16: 96,722-1,917,328 TPSG1, TPSP2, 110 more genes
    nsv3897602copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-1,875,694 , GRCh38.p12 chr16: 35,880-1,825,693 TPSG1, CHTF18, 110 more genes
    nsv3919625copy number variation1nstd102humanPathogenic GRCh38 chr16: 23,141-1,773,349 , NCBI36 chr16: 13,141-1,763,351 , GRCh37 chr16: 73,141-1,823,350 TPSG1, RHOT2, 106 more genes
    nsv3916129copy number variation1nstd102humanPathogenic NCBI36 chr16: 13,141-1,702,525 , GRCh38 chr16: 23,141-1,712,523 , GRCh37 chr16: 73,141-1,762,524 TPSG1, C4orf46P1, 102 more genes
    nsv3906615copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-1,715,454 , GRCh38.p12 chr16: 38,165-1,665,453 TPSG1, LOC105371046, 97 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