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Items: 1 to 20 of 314

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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
    nsv5972021copy number variation2nstd209human GRCh38 chrY: 14,020,998-14,119,394 , GRCh37.p13 chrY: 16,132,878-16,231,274 LOC100379236, PNPLA4P1, 1 more genes
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5665521inversion1nstd207human GRCh38 chrY: 13,984,161-14,058,526 , GRCh37.p13 chrY: 16,096,041-16,170,406 VCY, VCY1B
    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
    nsv5419788copy number variation1nstd206human GRCh38 chrY: 14,048,123-14,078,123 , GRCh37.p13 chrY: 16,160,003-16,190,003 VCY1B
    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
    nsv4674108copy number variation1nstd102humanUncertain significance GRCh37 chrY: 16,099,875-16,290,256 , GRCh38.p12 chrY: 13,987,995-14,178,376 VCY1B, LOC100379236, 1 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
    nsv4518191copy number variation1nstd166human GRCh37.p13 chrY: 16,152,999-16,361,500 , GRCh38.p12 chrY: 14,041,119-14,249,620 LOC100379236, VCY1B, 1 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
    nsv4451941copy number variation1nstd102humanPathogenic GRCh37 chrY: 16,053,146-59,343,488 , GRCh38.p12 chrY: 13,941,266-57,197,337 CD24P4, CSPG4P1Y, 327 more genes
    nsv4451757copy number variation1nstd102humanPathogenic GRCh37 chrY: 15,190,336-59,343,488 , GRCh38.p12 chrY: 13,078,422-57,197,337 DPH3P2, CDY16P, 337 more genes
    nsv4449745copy number variation1nstd102humanUncertain significance GRCh37 chrY: 16,099,875-16,702,276 , GRCh38.p12 chrY: 13,987,995-14,590,396 LOC100379236, VCY1B, 2 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
    nsv4384320copy number variation2nstd173human GRCh37 chrY: 15,990,012-16,171,568 , GRCh38.p12 chrY: 13,878,132-14,059,688 VCY, ANOS2P, 1 more genes
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