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 126

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094345copy number variation1nstd102humanUncertain significance GRCh37 chr14: 74,417,036-74,417,218 , GRCh38.p12 chr14: 73,950,333-73,950,515 FAM161B, COQ6
    nsv7060619inversion1nstd229human GRCh38 chr14: 73,833,212-74,127,471 , GRCh37.p13 chr14: 74,299,915-74,594,174 RPL41P4, ZNF410, 9 more genes
    nsv6960458copy number variation1nstd229human GRCh38 chr14: 73,932,859-73,937,174 , GRCh37.p13 chr14: 74,399,562-74,403,877 FAM161B, ZNF410
    nsv6482950copy number variation1nstd223human GRCh38 chr14: 73,949,561-73,951,530 , GRCh37.p13 chr14: 74,416,264-74,418,233 COQ6, FAM161B
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6132936copy number variation1nstd213human GRCh37 chr14: 73,480,000-74,470,001 , GRCh38.p12 chr14: 73,013,292-74,003,298 PSEN1, ACOT2, 32 more genes
    nsv6085428insertion1nstd212human GRCh38 chr14: 73,940,675-73,940,675 , GRCh37.p13 chr14: 74,407,378-74,407,378 FAM161B
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5720542mobile element insertion1nstd211human GRCh38 chr14: 73,943,384-73,943,384 , GRCh37.p13 chr14: 74,410,087-74,410,087 FAM161B
    nsv5554108mobile element insertion1nstd206human GRCh38 chr14: 73,943,384-73,943,435 , GRCh37.p13 chr14: 74,410,087-74,410,138 FAM161B
    nsv5504829copy number variation1nstd206human GRCh38 chr14: 73,949,384-73,951,523 , GRCh37.p13 chr14: 74,416,087-74,418,226 COQ6, FAM161B
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004789copy number variation1nstd200human GRCh38 chr14: 73,949,486-73,951,632 , GRCh37.p13 chr14: 74,416,189-74,418,335 COQ6, FAM161B
    nsv5004788copy number variation1nstd200human GRCh38 chr14: 73,948,251-73,982,556 , GRCh37.p13 chr14: 74,414,954-74,449,259 COQ6, ENTPD5, 1 more genes
    nsv4831347copy number variation1nstd200human GRCh37 chr14: 74,414,954-74,449,259 , GRCh38.p12 chr14: 73,948,251-73,982,556 FAM161B, COQ6, 1 more genes
    nsv4625674copy number variation1nstd183human GRCh37 chr14: 74,391,363-74,627,713 , GRCh38.p12 chr14: 73,924,660-74,161,010 RNY4P21, ZNF410, 8 more genes
    nsv4550143insertion1nstd166human GRCh37.p13 chr14: 74,409,443-74,409,443 , GRCh38.p12 chr14: 73,942,740-73,942,740 FAM161B
    nsv4451120copy number variation1nstd102humanUncertain significance GRCh38 chr14: 73,645,020-74,260,939 , GRCh37 chr14: 74,111,723-74,727,642 ENTPD5, COQ6, 20 more genes
    nsv4349747copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 74,040,231-76,368,547 , GRCh38.p12 chr14: 73,573,527-75,902,204 ACYP1, ENTPD5, 72 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