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 440

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117501copy number variation1nstd186human GRCh37 chr16: 1,292,001-1,304,001 , GRCh38.p12 chr16: 1,242,000-1,254,000 TPSAB1
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5978913inversion1nstd209human GRCh38 chr16: 1,239,856-1,248,248 , GRCh37.p13 chr16: 1,289,857-1,298,249 TPSAB1
    nsv5932159copy number variation1nstd209human GRCh38 chr16: 1,240,145-1,245,286 , GRCh37.p13 chr16: 1,290,146-1,295,287 TPSAB1
    nsv5670151inversion1nstd207human GRCh38 chr16: 1,226,689-1,255,753 , GRCh37.p13 chr16: 1,276,689-1,305,754 TPSAB1, TPSD1, 2 more genes
    nsv5428140copy number variation1nstd206human GRCh38 chr16: 1,242,000-1,254,000 , GRCh37.p13 chr16: 1,292,001-1,304,001 TPSAB1
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5335029translocation1nstd200human GRCh37 chr16: 1,290,146-1,290,146 , GRCh37 chr16: 1,295,288-1,295,288 , GRCh38.p12 chr16: 1,240,145-1,240,145 , GRCh38.p12 chr16: 1,245,287-1,245,287 TPSAB1
    nsv5311624copy number variation1nstd204human GRCh38.p13 chr16: 1,240,115-1,245,293 , GRCh37.p13 chr16: 1,290,116-1,295,294 TPSAB1
    nsv5278593copy number variation1nstd204human GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501 , MIR662, 73 more genes
    nsv5274418copy number variation1nstd204human GRCh38.p13 chr16: 1,237,601-1,254,500 , GRCh37.p13 chr16: 1,287,602-1,304,501 TPSD1, TPSAB1
    nsv5271242copy number variation1nstd204human GRCh38.p13 chr16: 1,226,901-1,255,100 , GRCh37.p13 chr16: 1,276,901-1,305,101 TPSAB1, TPSG1, 2 more genes
    nsv5267998copy number variation1nstd204human GRCh38.p13 chr16: 1,242,201-1,250,700 , GRCh37.p13 chr16: 1,292,202-1,300,701 TPSAB1
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5009337copy number variation1nstd200human GRCh38 chr16: 1,202,189-1,261,394 , GRCh37.p13 chr16: 1,252,189-1,311,395 TPSD1, PRSS29P, 4 more genes
    nsv4854326copy number variation1nstd200human GRCh37 chr16: 1,252,189-1,311,395 , GRCh38.p12 chr16: 1,202,189-1,261,394 TPSD1, TPSB2, 4 more genes
    nsv4757906inversion1nstd199human GRCh38.p12 chr16: 1,231,511-1,255,160 , GRCh37 chr16: 1,281,512-1,305,161 TPSAB1, TPSD1
    nsv4755323inversion1nstd199human GRCh38.p12 chr16: 1,236,420-1,250,074 , GRCh37 chr16: 1,286,421-1,300,075 TPSAB1
    nsv4751609inversion1nstd199human GRCh38.p12 chr16: 1,228,397-1,242,484 , GRCh37 chr16: 1,278,397-1,292,485 TPSAB1, TPSB2
    nsv4751135inversion1nstd199human GRCh38.p12 chr16: 1,233,761-1,252,665 , GRCh37 chr16: 1,283,762-1,302,666 TPSAB1
    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