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Items: 1 to 20 of 289

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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
    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
    nsv4909335copy number variation1nstd200human GRCh38 chrY: 13,552,782-14,021,543 , GRCh37.p13 chrY: 15,664,662-16,133,423 PSIP1P2, TMSB4Y, 2 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
    nsv4684038copy number variation1nstd102humanPathogenic GRCh37 chrY: 15,427,283-28,799,937 , GRCh38.p12 chrY: 13,315,403-26,653,790 LOC105377218, STSP1, 324 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
    nsv4517553copy number variation1nstd166human GRCh37.p13 chrY: 15,664,899-16,111,000 , GRCh38.p12 chrY: 13,553,019-13,999,120 PSIP1P2, TMSB4Y, 2 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
    nsv4451757copy number variation1nstd102humanPathogenic GRCh37 chrY: 15,190,336-59,343,488 , GRCh38.p12 chrY: 13,078,422-57,197,337 DPH3P2, CDY16P, 337 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
    nsv4384087copy number variation2nstd173human GRCh37 chrY: 15,660,045-16,171,585 , GRCh38.p12 chrY: 13,548,165-14,059,705 PSIP1P2, VCY1B, 3 more genes
    nsv4379979copy number variation1nstd173human GRCh37 chrY: 9,383,472-28,799,949 , GRCh38.p12 chrY: 9,545,863-26,653,802 , CSPG4P1Y, 400 more genes
    nsv4365247copy number variation1nstd173human GRCh37 chrY: 15,669,490-16,171,553 , GRCh38.p12 chrY: 13,557,610-14,059,673 VCY, ANOS2P, 3 more genes
    nsv4348642copy number variation1nstd102humanPathogenic GRCh37 chrY: 588,444-19,565,713 , GRCh38.p12 chrY: 677,709-17,453,833 TTTY2, ANKRD20A6P, 245 more genes
    nsv4348640copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,278-24,445,033 , GRCh38.p12 chrY: 2,782,237-22,298,886 CDY3P, USP9YP16, 357 more genes
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