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Items: 1 to 20 of 279

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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
    nsv4728217copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,069,286-5,727,224 , GRCh38.p12 chrY: 3,201,245-5,859,183 SERBP1P2, RNU2-57P, 16 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
    nsv4674653copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,037,424-5,739,448 , GRCh38.p12 chrY: 3,169,383-5,871,407 SERBP1P2, SNX3P1Y, 16 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
    nsv4511245copy number variation1nstd166human GRCh37.p13 chrY: 3,855,699-4,084,300 , GRCh38.p12 chrY: 3,987,658-4,216,259 RNU6-303P
    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
    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
    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
    nsv4036512copy number variation1nstd166human GRCh37.p13 chrY: 4,041,809-4,041,917 , GRCh38.p12 chrY: 4,173,768-4,173,876 RNU6-303P
    nsv3923512copy number variation1nstd102humanPathogenic NCBI36 chrY: 104,504-57,759,038 , GRCh37.p13 chrY: 114,504-59,349,650 , GRCh38.p12 chrY: 247,837-57,203,499 GPM6BP1, DAZ1, 568 more genes
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