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 331

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636057copy number variation1nstd102humanUncertain significance GRCh37 chrY: 16,203,971-59,336,737 , GRCh38.p12 chrY: 14,092,091-57,190,586 RBMY2YP, FAM8A9P, 324 more genes
    nsv6636003copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,370,813-59,373,566 , GRCh38.p12 chrY: 12,250,109-57,217,415 RBMY2FP, PRORY, 357 more genes
    nsv6634185copy number variation1nstd224human GRCh37 chrY: 16,913,677-24,522,333 , GRCh38.p12 chrY: 14,801,797-22,376,186 XKRY, CDY2A, 151 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315229copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 RBMY2VP, RFTN1P1, 570 more genes
    nsv6314745copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,424-28,799,654 , GRCh38.p12 chrY: 2,782,383-26,653,507 TTTY20, USP9YP18, 524 more genes
    nsv6314743copy number variation1nstd102humanPathogenic GRCh37 chrY: 13,905,421-28,799,654 , GRCh38.p12 chrY: 11,784,715-26,653,507 LOC102723934, RBMY1F, 348 more genes
    nsv6137649copy number variation2nstd213human GRCh37 chrY: 13,870,000-22,230,001 , GRCh38.p12 chrY: 11,749,294-20,068,115 ACTG1P2, ASS1P6, 132 more genes
    nsv6137648copy number variation1nstd213human GRCh37 chrY: 13,750,000-22,230,001 , GRCh38.p12 chrY: 11,677,873-20,068,115 ACTG1P2, ASS1P6, 132 more genes
    nsv6137647copy number variation1nstd213human GRCh37 chrY: 13,200,000-22,230,001 , GRCh38.p12 chrY: 11,044,324-20,068,115 ACTG1P2, ASS1P6, 153 more genes
    nsv6137418copy number variation1nstd213human GRCh37 chrY: 13,200,000-22,440,001 , GRCh38.p12 chrY: 11,044,324-20,278,115 ACTG1P2, ASS1P6, 153 more genes
    nsv6136807copy number variation1nstd213human GRCh37 chrY: 14,810,000-21,020,001 , GRCh38.p12 chrY: 12,698,071-18,858,115 ACTG1P2, ANOS2P, 102 more genes
    nsv6127496insertion1nstd186human GRCh37 chrY: 13,193,955-58,979,440 , GRCh38.p12 chrY: 11,038,279-56,833,293 , ELOCP10, 371 more genes
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5541060insertion1nstd206human GRCh38 chrY: 10,926,699-56,833,293 , GRCh37.p13 chrY: 13,193,955-58,979,440 , USP9YP18, 372 more genes
    nsv5432002copy number variation1nstd206human GRCh38 chrY: 17,451,387-18,881,388 , GRCh37.p13 chrY: 19,563,267-21,043,274 ACTG1P2, RNU1-95P, 75 more genes
    nsv5423876copy number variation1nstd206human GRCh38 chrY: 9,108,931-21,750,314 , GRCh37.p13 chrY: 8,964,956-23,901,428 , TSPY14P, 238 more genes
    nsv4730088inversion1nstd198human GRCh38 chrY: 18,172,892-18,292,282 , GRCh37.p13 chrY: 20,334,778-20,454,168 TAF9P2, CDY9P, 3 more genes
    nsv4684047copy number variation1nstd102humanPathogenic GRCh37 chrY: 13,800,703-28,799,937 , GRCh38.p12 chrY: 11,679,997-26,653,790 RBMY2VP, DNM1P24, 349 more genes
    nsv4684042copy number variation1nstd102humanPathogenic GRCh37 chrY: 18,546,605-28,799,937 , GRCh38.p12 chrY: 16,434,725-26,653,790 ANKRD36P1, LOC105377217, 305 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