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 204

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139115insertion1nstd232human GRCh37.p13 chr1: 100,527,506-100,527,506 , GRCh38.p12 chr1: 100,061,950-100,061,950 MFSD14A
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv7095681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008 SLC35A3, S1PR1-DT, 29 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6657977copy number variation1nstd229human GRCh38 chr1: 99,642,179-100,077,061 , GRCh37.p13 chr1: 100,107,735-100,542,617 MFSD14A, SLC35A3, 8 more genes
    nsv6657975copy number variation1nstd229human GRCh38 chr1: 99,498,947-100,487,486 , GRCh37.p13 chr1: 99,964,503-100,953,042 CDC14A, AGL, 21 more genes
    nsv6657529copy number variation1nstd229human GRCh38 chr1: 99,931,502-100,193,663 , GRCh37.p13 chr1: 100,397,058-100,659,219 DBT, TRMT13, 6 more genes
    nsv6657528copy number variation1nstd229human GRCh38 chr1: 99,924,501-100,058,000 , GRCh37.p13 chr1: 100,390,057-100,523,556 RNU6-1318P, MFSD14A, 3 more genes
    nsv6638164copy number variation1nstd229human GRCh38 chr1: 100,058,361-100,089,148 , GRCh37.p13 chr1: 100,523,917-100,554,704 MFSD14A, SASS6
    nsv6638163copy number variation1nstd229human GRCh38 chr1: 100,037,701-100,038,900 , GRCh37.p13 chr1: 100,503,257-100,504,456 MFSD14A
    nsv6551917inversion1nstd223human GRCh38 chr1: 100,051,086-100,052,692 , GRCh37.p13 chr1: 100,516,642-100,518,248 MFSD14A
    nsv6548592inversion1nstd223human GRCh38 chr1: 100,041,642-100,042,907 , GRCh37.p13 chr1: 100,507,198-100,508,463 MFSD14A
    nsv6332598copy number variation1nstd223human GRCh38 chr1: 99,642,179-100,077,059 , GRCh37.p13 chr1: 100,107,735-100,542,615 HMGB3P10, RNU6-750P, 8 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6290366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608 LOC105379827, RPSAP19, 63 more genes
    nsv6133891copy number variation1nstd213human GRCh37 chr1: 99,980,000-100,540,001 , GRCh38.p12 chr1: 99,514,444-100,074,445 AGL, SLC35A3, 8 more genes
    nsv6133669copy number variation1nstd213human GRCh37 chr1: 95,900,000-101,030,001 , GRCh38.p12 chr1: 95,434,444-100,564,445 PALMD, LRRC39, 56 more genes
    nsv5827765copy number variation1nstd209human GRCh38 chr1: 100,052,414-100,055,638 , GRCh37.p13 chr1: 100,517,970-100,521,194 MFSD14A
    nsv5687206mobile element insertion1nstd211human GRCh38 chr1: 100,060,061-100,060,061 , GRCh37.p13 chr1: 100,525,617-100,525,617 MFSD14A
    nsv5431994copy number variation1nstd206human GRCh38 chr1: 100,052,425-100,055,832 , GRCh37.p13 chr1: 100,517,981-100,521,388 MFSD14A
    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