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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636003copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,370,813-59,373,566 , GRCh38.p12 chrY: 12,250,109-57,217,415 RBMY2FP, PRORY, 357 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315229copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 RBMY2VP, RFTN1P1, 570 more genes
    nsv6314745copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,424-28,799,654 , GRCh38.p12 chrY: 2,782,383-26,653,507 TTTY20, USP9YP18, 524 more genes
    nsv6314743copy number variation1nstd102humanPathogenic GRCh37 chrY: 13,905,421-28,799,654 , GRCh38.p12 chrY: 11,784,715-26,653,507 LOC102723934, RBMY1F, 348 more genes
    nsv6137649copy number variation2nstd213human GRCh37 chrY: 13,870,000-22,230,001 , GRCh38.p12 chrY: 11,749,294-20,068,115 ACTG1P2, ASS1P6, 132 more genes
    nsv6137648copy number variation1nstd213human GRCh37 chrY: 13,750,000-22,230,001 , GRCh38.p12 chrY: 11,677,873-20,068,115 ACTG1P2, ASS1P6, 132 more genes
    nsv6137647copy number variation1nstd213human GRCh37 chrY: 13,200,000-22,230,001 , GRCh38.p12 chrY: 11,044,324-20,068,115 ACTG1P2, ASS1P6, 153 more genes
    nsv6137419copy number variation1nstd213human GRCh37 chrY: 14,810,000-19,950,001 , GRCh38.p12 chrY: 12,698,071-17,838,121 ACTG1P2, ANOS2P, 48 more genes
    nsv6137418copy number variation1nstd213human GRCh37 chrY: 13,200,000-22,440,001 , GRCh38.p12 chrY: 11,044,324-20,278,115 ACTG1P2, ASS1P6, 153 more genes
    nsv6137238copy number variation1nstd213human GRCh37 chrY: 13,870,000-20,030,001 , GRCh38.p12 chrY: 11,749,294-17,918,121 ACTG1P2, ASS1P6, 68 more genes
    nsv6136807copy number variation1nstd213human GRCh37 chrY: 14,810,000-21,020,001 , GRCh38.p12 chrY: 12,698,071-18,858,115 ACTG1P2, ANOS2P, 102 more genes
    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
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