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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127496insertion1nstd186human GRCh37 chrY: 13,193,955-58,979,440 , GRCh38.p12 chrY: 11,038,279-56,833,293 , ELOCP10, 371 more genes
    nsv5973707copy number variation1nstd209human GRCh38 chrY: 12,782,246-12,785,145 , GRCh37.p13 chrY: 14,894,180-14,897,079 USP9Y
    nsv5885258copy number variation1nstd209human GRCh38 chrY: 12,782,845-12,784,885 , GRCh37.p13 chrY: 14,894,779-14,896,819 USP9Y
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5622048insertion1nstd207human GRCh38 chrY: 12,835,615-12,835,615 , GRCh37.p13 chrY: 14,947,541-14,947,541 USP9Y
    nsv5541060insertion1nstd206human GRCh38 chrY: 10,926,699-56,833,293 , GRCh37.p13 chrY: 13,193,955-58,979,440 , USP9YP18, 372 more genes
    nsv5429795copy number variation1nstd206human GRCh38 chrY: 12,782,845-12,784,897 , GRCh37.p13 chrY: 14,894,779-14,896,831 USP9Y
    nsv5423876copy number variation1nstd206human GRCh38 chrY: 9,108,931-21,750,314 , GRCh37.p13 chrY: 8,964,956-23,901,428 , TSPY14P, 238 more genes
    nsv5419381copy number variation1nstd206human GRCh38 chrY: 11,944,532-13,195,289 , GRCh37.p13 chrY: 14,065,238-15,307,187 , SFPQP1, 20 more genes
    nsv5380422translocation1nstd200human GRCh38 chrY: 12,782,845-12,782,845 , GRCh38 chrY: 12,784,895-12,784,895 , GRCh37.p13 chrY: 14,894,779-14,894,779 , GRCh37.p13 chrY: 14,896,829-14,896,829 USP9Y
    nsv4909331copy number variation1nstd200human GRCh38 chrY: 12,372,623-12,743,377 , GRCh37.p13 chrY: 14,491,216-14,855,311 , TTTY15, 7 more genes
    nsv4902893copy number variation1nstd200human GRCh38 chrY: 12,824,743-12,898,619 , GRCh37.p13 chrY: 14,936,678-15,010,534 USP9Y
    nsv4788111copy number variation1nstd200human GRCh37 chrY: 14,936,678-15,010,534 , GRCh38.p12 chrY: 12,824,743-12,898,619 USP9Y
    nsv4788110copy number variation1nstd200human GRCh37 chrY: 14,894,779-14,896,831 , GRCh38.p12 chrY: 12,782,845-12,784,897 USP9Y
    nsv4782464copy number variation1nstd200human GRCh37 chrY: 14,113,955-15,528,681 , GRCh38.p12 chrY: 11,993,249-13,416,801 , LOC112268311, 22 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
    nsv4684020copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,495,040-24,070,172 , GRCh38.p12 chrY: 12,383,237-21,924,025 TMEM167AP1, ELOCP13, 157 more genes
    nsv4674763copy number variation1nstd102humanUncertain significance GRCh37 chrY: 14,787,490-14,996,799 , GRCh38.p12 chrY: 12,675,560-12,884,884 USP9Y, CDY4P, 1 more genes
    nsv4674019copy number variation1nstd102humanUncertain significance GRCh37 chrY: 14,853,163-15,454,303 , GRCh38.p12 chrY: 12,741,229-13,342,423 UTY, PSMA6P1, 8 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
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