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Items: 1 to 20 of 328

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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
    nsv5976981copy number variation1nstd209human GRCh38 chrY: 12,390,193-12,408,233 , GRCh37.p13 chrY: 14,501,988-14,520,032 , GYG2P1
    nsv5975464copy number variation1nstd209human GRCh38 chrY: 12,378,990-12,554,562 , GRCh37.p13 chrY: 14,491,216-14,666,496 , XGY1, 3 more genes
    nsv5672489copy number variation1nstd207human GRCh38 chrY: 12,418,752-12,419,252 , GRCh37.p13 chrY: 14,530,551-14,531,051 GYG2P1
    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
    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
    nsv5377346translocation1nstd200human GRCh38 chrY: 12,360,944-12,360,944 , GRCh38 chrY: 12,405,878-12,405,878 , GRCh37.p13 chrY: 14,481,675-14,481,675 , GRCh37.p13 chrY: 14,517,677-14,517,677 ARSDP1, GYG2P1, 1 more genes
    nsv5341657translocation1nstd200human GRCh37 chrY: 14,517,677-14,517,677 , GRCh37 chrY: 14,481,675-14,481,675 , GRCh38.p12 chrY: 12,405,878-12,405,878 , GRCh38.p12 chrY: 12,360,944-12,360,944 ARSDP1, GYG2P1, 1 more genes
    nsv4909331copy number variation1nstd200human GRCh38 chrY: 12,372,623-12,743,377 , GRCh37.p13 chrY: 14,491,216-14,855,311 , TTTY15, 7 more genes
    nsv4902890copy number variation1nstd200human GRCh38 chrY: 12,416,787-12,417,448 , GRCh37.p13 chrY: 14,528,586-14,529,247 GYG2P1
    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
    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
    nsv4673916copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,486,671-15,098,073 , GRCh38.p12 chrY: 12,365,940-12,986,161 MED14P1, CDY4P, 9 more genes
    nsv4517852copy number variation1nstd166human GRCh37.p13 chrY: 14,447,397-14,558,056 , GRCh38.p12 chrY: 12,326,670-12,446,257 , LOC107987343, 3 more genes
    nsv4517109copy number variation1nstd166human GRCh37.p13 chrY: 13,978,999-14,760,100 , GRCh38.p12 chrY: 11,858,293-12,648,169 , ARSLP1, 12 more genes
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