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 137

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077997inversion1nstd229human GRCh38 chr19: 50,085,764-53,270,581 , GRCh37.p13 chr19: 50,589,021-53,773,834 SNORD88B, ZNF320, 181 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7069681inversion1nstd229human GRCh38 chr19: 50,654,313-52,443,676 , GRCh37.p13 chr19: 51,157,570-52,946,929 CTU1, LOC100419835, 117 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7012578copy number variation1nstd229human GRCh38 chr19: 51,747,919-51,750,119 , GRCh37.p13 chr19: 52,251,172-52,253,372 FPR2, FPR1
    nsv7011442copy number variation1nstd229human GRCh38 chr19: 51,747,008-51,751,812 , GRCh37.p13 chr19: 52,250,261-52,255,065 FPR2, FPR1
    nsv7010498copy number variation1nstd229human GRCh38 chr19: 51,721,256-51,857,363 , GRCh37.p13 chr19: 52,224,509-52,360,616 ZNF577, HAS1, 5 more genes
    nsv7010293copy number variation1nstd229human GRCh38 chr19: 51,744,187-51,756,247 , GRCh37.p13 chr19: 52,247,440-52,259,500 FPR2, FPR1
    nsv6999838copy number variation1nstd229human GRCh38 chr19: 51,747,006-51,750,201 , GRCh37.p13 chr19: 52,250,259-52,253,454 FPR1, FPR2
    nsv6596265inversion1nstd223human GRCh38 chr19: 51,744,243-51,745,250 , GRCh37.p13 chr19: 52,247,496-52,248,503 FPR1
    nsv6519823copy number variation1nstd223human GRCh38 chr19: 51,745,501-51,747,200 , GRCh37.p13 chr19: 52,248,754-52,250,453 FPR1
    nsv6518554copy number variation1nstd223human GRCh38 chr19: 51,721,256-51,857,352 , GRCh37.p13 chr19: 52,224,509-52,360,605 FPR1, ZNF577, 5 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6310492copy number variation1nstd102humanUncertain significance GRCh37 chr19: 52,249,195-52,250,247 , GRCh38.p12 chr19: 51,745,942-51,746,994 FPR1
    nsv6291759copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,769,834-52,415,762 , GRCh38.p12 chr19: 51,266,580-51,912,509 ZNF649-AS1, SIGLEC12, 46 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5708653mobile element insertion1nstd211human GRCh38 chr19: 51,744,650-51,744,650 , GRCh37.p13 chr19: 52,247,903-52,247,903 FPR1
    nsv5703752mobile element insertion1nstd211human GRCh38 chr19: 51,744,677-51,744,677 , GRCh37.p13 chr19: 52,247,930-52,247,930 FPR1
    nsv5518208copy number variation1nstd206human GRCh38 chr19: 51,749,200-51,753,624 , GRCh37.p13 chr19: 52,252,453-52,256,877 FPR2, FPR1
    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