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Items: 1 to 20 of 286

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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
    nsv5431206copy number variation1nstd206human GRCh38 chrY: 6,266,388-9,335,488 , GRCh37.p13 chrY: 6,134,429-9,173,097 , RN7SKP282, 76 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
    nsv4909324copy number variation1nstd200human GRCh38 chrY: 9,162,169-9,268,779 , GRCh37.p13 chrY: 8,999,778-9,106,388 USP9YP4, ELOCP4, 3 more genes
    nsv4909322copy number variation1nstd200human GRCh38 chrY: 8,991,407-9,282,879 , GRCh37.p13 chrY: 8,859,448-9,120,488 USP9YP4, LOC105379265, 5 more genes
    nsv4730219inversion4nstd198human GRCh38 chrY: 6,198,014-9,936,872 , GRCh37.p13 chrY: 6,066,055-9,774,481 , AMELY, 109 more genes
    nsv4674023copy number variation1nstd102humanUncertain significance GRCh37 chrY: 6,135,412-9,155,562 , GRCh38.p12 chrY: 6,267,371-9,317,953 MTND2P3, TBL1Y, 73 more genes
    nsv4674007copy number variation1nstd102humanLikely benign GRCh37 chrY: 6,172,777-9,168,128 , GRCh38.p12 chrY: 6,304,736-9,330,519 TSPY12P, GOT2P5, 74 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
    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
    nsv4385524copy number variation3nstd173human GRCh37 chrY: 2,650,141-28,799,949 , GRCh38.p12 chrY: 2,782,100-26,653,802 , MTND1P12, 527 more genes
    nsv4381780copy number variation1nstd173human GRCh37 chrY: 6,165,770-9,305,278 , GRCh38.p12 chrY: 6,297,729-9,467,669 , ATP5PFP1, 84 more genes
    nsv4372867copy number variation1nstd173human GRCh37 chrY: 6,120,598-9,168,156 , GRCh38.p12 chrY: 6,252,557-9,330,547 , LINC00280, 77 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
    nsv4348629copy number variation1nstd102humanPathogenic GRCh37 chrY: 1,640,371-19,565,713 , GRCh38.p12 chrY: 1,571,478-17,453,833 FAM197Y2, RBMY1A3P, 231 more genes
    nsv3969695inversion1nstd168human GRCh38 chrY: 6,224,711-9,917,945 , GRCh37.p13 chrY: 6,092,752-9,755,554 , AMELY, 109 more genes
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