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 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139377copy number variation1nstd232human GRCh37.p13 chr19: 36,605,153-36,605,239 , GRCh38.p12 chr19: 36,114,251-36,114,337 TBCB, POLR2I
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7006389copy number variation1nstd229human GRCh38 chr19: 36,123,553-36,133,340 , GRCh37.p13 chr19: 36,614,455-36,624,242 LOC105372385, TBCB
    nsv7006224copy number variation1nstd229human GRCh38 chr19: 36,115,973-36,116,270 , GRCh37.p13 chr19: 36,606,875-36,607,172 TBCB
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005456copy number variation1nstd229human GRCh38 chr19: 35,863,391-36,727,332 , GRCh37.p13 chr19: 36,354,293-37,218,234 ZNF146, CLIP3, 39 more genes
    nsv7000686copy number variation1nstd229human GRCh38 chr19: 36,094,511-36,127,632 , GRCh37.p13 chr19: 36,585,413-36,618,534 POLR2I, LOC105372385, 3 more genes
    nsv6999792copy number variation1nstd229human GRCh38 chr19: 36,044,743-36,166,690 , GRCh37.p13 chr19: 36,535,645-36,657,592 LOC105372385, COX7A1, 8 more genes
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6145427copy number variation1nstd206human GRCh38 chr19: 36,016,874-36,114,874 , GRCh37.p13 chr19: 36,507,776-36,605,776 TBCB, POLR2I, 6 more genes
    nsv6133701copy number variation1nstd213human GRCh37 chr19: 36,490,000-36,640,001 , GRCh38.p12 chr19: 35,999,098-36,149,099 CAPNS1, TBCB, 11 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5729478mobile element insertion2nstd211human GRCh38 chr19: 36,126,419-36,126,419 , GRCh37.p13 chr19: 36,617,321-36,617,321 LOC105372385, TBCB
    nsv5644711insertion1nstd207human GRCh38 chr19: 36,126,419-36,126,419 , GRCh37.p13 chr19: 36,617,321-36,617,321 LOC105372385, TBCB
    nsv5323121translocation1nstd204human GRCh38.p13 chr19: 36,118,731-36,118,731 , GRCh38.p13 chr19: 36,118,613-36,118,613 , GRCh37.p13 chr19: 36,609,633-36,609,633 , GRCh37.p13 chr19: 36,609,515-36,609,515 TBCB
    nsv5289021copy number variation1nstd204human GRCh38.p13 chr19: 36,002,801-36,145,200 , GRCh37.p13 chr19: 36,493,703-36,636,102 LOC101927572, THAP8, 10 more genes
    nsv5198422mobile element insertion1nstd203human GRCh38 chr19: 36,126,370-36,126,419 , GRCh37.p13 chr19: 36,617,272-36,617,321 LOC105372385, TBCB
    nsv5197308mobile element insertion1nstd203human GRCh38 chr19: 36,126,415-36,126,419 , GRCh37.p13 chr19: 36,617,317-36,617,321 TBCB, LOC105372385
    nsv5193009mobile element insertion1nstd203human GRCh38 chr19: 36,126,424-36,126,424 , GRCh37.p13 chr19: 36,617,326-36,617,326 LOC105372385, TBCB
    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