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 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131470insertion1nstd186human GRCh37 chr19: 41,849,848-41,849,872 , GRCh38.p12 chr19: 41,343,943-41,343,967 TGFB1
    nsv5947320copy number variation1nstd209human GRCh38 chr19: 41,341,050-41,341,319 , GRCh37.p13 chr19: 41,846,955-41,847,224 TGFB1
    nsv5537927insertion1nstd206human GRCh38 chr19: 41,343,943-41,343,967 , GRCh37.p13 chr19: 41,849,848-41,849,872 TGFB1
    nsv5516161copy number variation1nstd206human GRCh38 chr19: 41,338,281-41,338,680 , GRCh37.p13 chr19: 41,844,186-41,844,585 TGFB1
    nsv5288731copy number variation1nstd204human GRCh38.p13 chr19: 41,182,901-41,435,300 , GRCh37.p13 chr19: 41,688,806-41,936,866 LOC105372401, AXL, 13 more genes
    nsv5024653copy number variation1nstd200human GRCh38 chr19: 41,351,628-41,450,794 , GRCh37.p13 chr19: 41,857,533-41,936,866 BCKDHA, B9D2, 7 more genes
    nsv5024652copy number variation1nstd200human GRCh38 chr19: 41,335,976-41,337,282 , GRCh37.p13 chr19: 41,841,881-41,843,187 TGFB1
    nsv5020480copy number variation1nstd200human GRCh38 chr19: 41,346,868-41,350,445 , GRCh37.p13 chr19: 41,852,773-41,856,350 TGFB1
    nsv5020479copy number variation1nstd200human GRCh38 chr19: 41,334,513-41,335,123 , GRCh37.p13 chr19: 41,840,418-41,841,028 TGFB1
    nsv4868410copy number variation1nstd200human GRCh37 chr19: 41,840,417-41,841,026 , GRCh38.p12 chr19: 41,334,512-41,335,121 TGFB1
    nsv4865179copy number variation1nstd200human GRCh37 chr19: 41,857,533-41,956,699 , GRCh38.p12 chr19: 41,351,628-41,450,794 B9D2, BCKDHA, 7 more genes
    nsv4769821mobile element deletion1nstd200human GRCh37 chr19: 41,853,480-41,853,764 , GRCh38.p12 chr19: 41,347,575-41,347,859 TGFB1
    nsv4719556insertion1nstd186human GRCh37 chr19: 41,849,799-41,849,799 , GRCh38.p12 chr19: 41,343,894-41,343,894 TGFB1
    nsv4676245copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,304,025-41,928,997 , GRCh38.p12 chr19: 40,798,120-41,423,092 CYP2T1P, RN7SL34P, 26 more genes
    nsv4549499insertion1nstd166human GRCh37.p13 chr19: 41,849,799-41,849,799 , GRCh38.p12 chr19: 41,343,894-41,343,894 TGFB1
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4264142copy number variation1nstd166human GRCh37.p13 chr19: 41,851,775-41,853,993 , GRCh38.p12 chr19: 41,345,870-41,348,088 TGFB1
    nsv4262728copy number variation1nstd166human GRCh37.p13 chr19: 41,851,524-41,874,793 , GRCh38.p12 chr19: 41,345,619-41,368,888 TGFB1, TMEM91, 1 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    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