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 205

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072983inversion1nstd229human GRCh38 chr17: 79,606,852-81,315,890 , GRCh37.p13 chr17: 77,766,017-79,289,690 MIR4739, MIR4730, 44 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv7067212inversion1nstd229human GRCh38 chr17: 79,320,851-81,127,081 , GRCh37.p13 chr17: 77,316,933-79,100,881 RPL32P31, RPTOR, 35 more genes
    nsv7065384inversion1nstd229human GRCh38 chr17: 79,173,003-81,030,493 , GRCh37.p13 chr17: 77,169,085-79,004,293 GAA, ENPP7, 30 more genes
    nsv7061803inversion1nstd229human GRCh38 chr17: 79,169,515-81,031,248 , GRCh37.p13 chr17: 77,165,597-79,005,048 CBX4, SLC26A11, 30 more genes
    nsv6997851copy number variation1nstd229human GRCh38 chr17: 80,998,855-81,006,722 , GRCh37.p13 chr17: 78,972,655-78,980,522 CHMP6
    nsv6993667copy number variation1nstd229human GRCh38 chr17: 78,709,580-81,173,842 , GRCh37.p13 chr17: 76,705,662-79,147,642 C1QTNF1-AS1, NPTX1, 47 more genes
    nsv6982359copy number variation1nstd229human GRCh38 chr17: 80,975,523-80,991,478 , GRCh37.p13 chr17: 78,949,323-78,965,278 RPL12P37, CHMP6
    nsv6637686copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,230,693-79,048,694 , GRCh38.p12 chr17: 80,256,894-81,074,894 RNF213-AS1, RPL31P7, 13 more genes
    nsv6637575copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,502,408-79,065,152 , GRCh38.p12 chr17: 80,528,608-81,091,352 LOC101928855, LOC400627, 8 more genes
    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
    nsv6314160copy number variation1nstd102humanUncertain significance GRCh37 chr17: 77,641,336-79,465,235 , GRCh38.p12 chr17: 79,667,474-81,498,209 BAIAP2-DT, SLC38A10, 49 more genes
    nsv6188748copy number variation1nstd214human GRCh38 chr17: 80,994,786-80,994,894 , GRCh37.p13 chr17: 78,968,586-78,968,694 CHMP6
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6098063insertion1nstd212human GRCh38 chr17: 80,994,908-80,994,908 , GRCh37.p13 chr17: 78,968,708-78,968,708 CHMP6
    nsv6025220copy number variation1nstd212human GRCh38 chr17: 80,994,725-80,994,802 , GRCh37.p13 chr17: 78,968,525-78,968,602 CHMP6
    nsv5971582insertion1nstd209human GRCh38 chr17: 80,997,355-80,997,355 , GRCh37.p13 chr17: 78,971,155-78,971,155 CHMP6
    nsv5657296insertion1nstd207human GRCh38 chr17: 80,994,696-80,994,696 , GRCh37.p13 chr17: 78,968,496-78,968,496 CHMP6
    nsv5586580copy number variation1nstd207human GRCh38 chr17: 80,994,696-80,994,773 , GRCh37.p13 chr17: 78,968,496-78,968,573 CHMP6
    nsv5527427copy number variation1nstd206human GRCh38 chr17: 80,661,347-81,015,738 , GRCh37.p13 chr17: 78,635,147-78,989,538 , RPTOR, 6 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