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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5431133copy number variation1nstd206human GRCh38 chrY: 2,781,388-3,953,388 , GRCh37.p13 chrY: 2,649,429-3,821,429 UBE2V1P3, LOC105377227, 17 more genes
    nsv4728687copy number variation1nstd102humanUncertain significance GRCh37 chrY: 1,873,925-2,800,880 , GRCh38.p12 chrY: 1,805,032-2,932,839 HSFY3P, NAP1L1P2, 14 more genes
    nsv4684050copy number variation1nstd102humanPathogenic GRCh38.p12 chrY: 2,782,099-2,909,476 , GRCh37 chrY: 2,650,140-2,777,517 RPS4Y1, SRY, 4 more genes
    nsv4684048copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-6,367,818 , GRCh38.p12 chrY: 2,782,099-6,499,777 SNX3P1Y, LOC100533723, 42 more genes
    nsv4684046copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-7,019,586 , GRCh38.p12 chrY: 2,782,099-7,151,545 KRT18P10, TTTY23B, 50 more genes
    nsv4684040copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-6,172,892 , GRCh38.p12 chrY: 2,782,099-6,304,851 ZFY, TGIF2LY, 34 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
    nsv4576116mobile element insertion1nstd166human GRCh37.p13 chrY: 2,654,319-2,654,319 , GRCh38.p12 chrY: 2,786,278-2,786,278 SRY
    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
    nsv4386001copy number variation1nstd173human GRCh37 chrY: 2,650,141-2,829,678 , GRCh38.p12 chrY: 2,782,100-2,961,637 SRY, RNASEH2CP1, 6 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
    nsv4382450copy number variation1nstd173human GRCh37 chrY: 2,650,141-2,725,140 , GRCh38.p12 chrY: 2,782,100-2,857,099 RNASEH2CP1, TOMM22P2, 3 more genes
    nsv4368232copy number variation1nstd173human GRCh37 chrY: 2,650,141-2,841,955 , GRCh38.p12 chrY: 2,782,100-2,973,914 NAP1L1P2, ZFY, 7 more genes
    nsv4368051copy number variation1nstd173human GRCh37 chrY: 2,650,141-6,114,797 , GRCh38.p12 chrY: 2,782,100-6,246,756 TGIF2LY, ZFY, 31 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
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