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 287

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7145395insertion1nstd232human GRCh37.p13 chr17: 74,036,016-74,036,016 , GRCh38.p12 chr17: 76,039,935-76,039,935 SRP68
    nsv7138909insertion1nstd232human GRCh37.p13 chr17: 74,053,625-74,053,625 , GRCh38.p12 chr17: 76,057,544-76,057,544 SRP68
    nsv7138068insertion1nstd232human GRCh37.p13 chr17: 74,057,304-74,057,304 , GRCh38.p12 chr17: 76,061,223-76,061,223 SRP68
    nsv7065329inversion1nstd229human GRCh38 chr17: 75,958,231-76,360,906 , GRCh37.p13 chr17: 73,954,312-74,356,987 RNF157, ACOX1, 20 more genes
    nsv6994010copy number variation1nstd229human GRCh38 chr17: 76,052,230-76,053,221 , GRCh37.p13 chr17: 74,048,311-74,049,302 SRP68
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6982623copy number variation1nstd229human GRCh38 chr17: 76,027,183-76,050,670 , GRCh37.p13 chr17: 74,023,264-74,046,751 EVPL, SRP68
    nsv6978614copy number variation1nstd229human GRCh38 chr17: 76,038,335-76,038,403 , GRCh37.p13 chr17: 74,034,416-74,034,484 SRP68
    nsv6585468inversion1nstd223human GRCh38 chr17: 76,054,762-76,054,946 , GRCh37.p13 chr17: 74,050,843-74,051,027 SRP68
    nsv6585076inversion1nstd223human GRCh38 chr17: 76,058,095-76,059,170 , GRCh37.p13 chr17: 74,054,176-74,055,251 SRP68
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6577537inversion1nstd223human GRCh38 chr17: 76,054,572-76,055,170 , GRCh37.p13 chr17: 74,050,653-74,051,251 SRP68
    nsv6521087copy number variation1nstd223human GRCh38 chr17: 76,059,789-76,063,688 , GRCh37.p13 chr17: 74,055,870-74,059,769 SRP68
    nsv6517213copy number variation1nstd223human GRCh38 chr17: 76,012,912-76,062,933 , GRCh37.p13 chr17: 74,008,993-74,059,014 SRP68, EVPL
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6259079mobile element insertion1nstd215human GRCh38 chr17: 76,050,743-76,050,743 , GRCh37.p13 chr17: 74,046,824-74,046,824 SRP68
    nsv6084365insertion1nstd212human GRCh38 chr17: 76,065,273-76,065,273 , GRCh37.p13 chr17: 74,061,354-74,061,354 SRP68
    nsv6082816insertion1nstd212human GRCh38 chr17: 76,062,669-76,062,669 , GRCh37.p13 chr17: 74,058,750-74,058,750 SRP68
    nsv6081173insertion1nstd212human GRCh38 chr17: 76,050,728-76,050,728 , GRCh37.p13 chr17: 74,046,809-74,046,809 SRP68
    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