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 305

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885382copy number variation1nstd209human GRCh38 chrY: 8,806,452-8,806,639 , GRCh37.p13 chrY: 8,674,493-8,674,680 TTTY11
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5431206copy number variation1nstd206human GRCh38 chrY: 6,266,388-9,335,488 , GRCh37.p13 chrY: 6,134,429-9,173,097 , RN7SKP282, 76 more genes
    nsv5380405translocation1nstd200human GRCh38 chrY: 8,807,447-8,807,447 , GRCh38 chrY: 8,807,344-8,807,344 , GRCh37.p13 chrY: 8,675,488-8,675,488 , GRCh37.p13 chrY: 8,675,385-8,675,385 TTTY11
    nsv5380404translocation1nstd200human GRCh38 chrY: 8,806,453-8,806,453 , GRCh38 chrY: 8,806,640-8,806,640 , GRCh37.p13 chrY: 8,674,681-8,674,681 , GRCh37.p13 chrY: 8,674,494-8,674,494 TTTY11
    nsv5200253mobile element insertion1nstd203human GRCh38 chrY: 8,790,134-8,790,150 , GRCh37.p13 chrY: 8,658,175-8,658,191 TTTY11
    nsv4788087copy number variation1nstd200human GRCh37 chrY: 8,675,385-8,675,488 , GRCh38.p12 chrY: 8,807,344-8,807,447 TTTY11
    nsv4788086copy number variation1nstd200human GRCh37 chrY: 8,674,494-8,674,681 , GRCh38.p12 chrY: 8,806,453-8,806,640 TTTY11
    nsv4782461copy number variation1nstd200human GRCh37 chrY: 8,663,115-8,675,377 , GRCh38.p12 chrY: 8,795,074-8,807,336 TTTY11
    nsv4782460copy number variation1nstd200human GRCh37 chrY: 8,201,953-8,675,412 , GRCh38.p12 chrY: 8,333,912-8,807,371 LOC107987354, MTND1P1, 17 more genes
    nsv4782459copy number variation1nstd200human GRCh37 chrY: 8,201,996-8,663,170 , GRCh38.p12 chrY: 8,333,955-8,795,129 LOC105377234, TTTY27P, 17 more genes
    nsv4730219inversion4nstd198human GRCh38 chrY: 6,198,014-9,936,872 , GRCh37.p13 chrY: 6,066,055-9,774,481 , AMELY, 109 more genes
    nsv4674023copy number variation1nstd102humanUncertain significance GRCh37 chrY: 6,135,412-9,155,562 , GRCh38.p12 chrY: 6,267,371-9,317,953 MTND2P3, TBL1Y, 73 more genes
    nsv4674007copy number variation1nstd102humanLikely benign GRCh37 chrY: 6,172,777-9,168,128 , GRCh38.p12 chrY: 6,304,736-9,330,519 TSPY12P, GOT2P5, 74 more genes
    nsv4673949copy number variation1nstd102humanPathogenic GRCh37 chrY: 168,546-28,799,937 , GRCh38.p12 chrY: 301,879-26,653,790 GPM6BP2, TTTY18, 559 more genes
    nsv4673928copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-16,095,773 , GRCh38.p12 chrY: 10,001-13,983,893 TTTY21, MTCO3P37, 239 more genes
    nsv4454174copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-20,619,847 , GRCh38.p12 chrY: 2,782,099-18,457,961 ZNF736P8Y, FAM197Y7, 269 more genes
    nsv4451989copy number variation1nstd102humanPathogenic GRCh37 chrY: 118,546-20,603,124 , GRCh38.p12 chrY: 251,879-18,441,238 LOC107985677, SOWAHCP1, 303 more genes
    nsv4451304copy number variation1nstd102humanPathogenic GRCh37 chrY: 201,704-15,182,563 , GRCh38.p12 chrY: 320,650-13,070,649 NAP1L1P2, AGPAT5P1, 226 more genes
    nsv4385524copy number variation3nstd173human GRCh37 chrY: 2,650,141-28,799,949 , GRCh38.p12 chrY: 2,782,100-26,653,802 , MTND1P12, 527 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