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Items: 1 to 20 of 331

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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
    nsv5419381copy number variation1nstd206human GRCh38 chrY: 11,944,532-13,195,289 , GRCh37.p13 chrY: 14,065,238-15,307,187 , SFPQP1, 20 more genes
    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
    nsv4674019copy number variation1nstd102humanUncertain significance GRCh37 chrY: 14,853,163-15,454,303 , GRCh38.p12 chrY: 12,741,229-13,342,423 UTY, PSMA6P1, 8 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
    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
    nsv4379979copy number variation1nstd173human GRCh37 chrY: 9,383,472-28,799,949 , GRCh38.p12 chrY: 9,545,863-26,653,802 , CSPG4P1Y, 400 more genes
    nsv4348735copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrY: 14,443,478-15,230,544 , GRCh38.p12 chrY: 12,322,751-13,118,630 ARSDP1, GYG2P1, 14 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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