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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895011copy number variation1nstd102humanconflicting data from submitters GRCh37 chr14: 35,734,798-35,784,055 , GRCh38.p12 chr14: 35,265,592-35,314,849 PSMA6, PRORP
    nsv4673876copy number variation1nstd102humanLikely benign GRCh37 chrY: 15,230,542-15,504,417 , GRCh38.p12 chrY: 13,118,628-13,392,537 PSMA6P1, DPPA2P1, 3 more genes
    nsv4728195copy number variation1nstd102humanLikely benign GRCh37 chrY: 15,230,542-15,491,487 , GRCh38.p12 chrY: 13,118,628-13,379,607 DPPA2P1, UTY, 3 more genes
    nsv4456501copy number variation1nstd102humanUncertain significance GRCh37 chr14: 35,724,243-35,850,214 , GRCh38.p12 chr14: 35,255,037-35,381,008 PSMA6, PRORP, 1 more genes
    nsv3913268copy number variation1nstd102humanPathogenic NCBI36 chrY: 679-57,764,265 , GRCh37.p13 chrY: 10,679-59,354,877 , GRCh38.p12 chrY: 10,679-57,208,726 DNM1P24, RNA5SP498, 569 more genes
    nsv3889933copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-59,349,277 , GRCh38.p12 chrY: 10,701-57,203,126 PPP2R3B, ASMT, 568 more genes
    nsv3881186copy number variation1nstd102humanPathogenic GRCh37 chrY: 20,297-59,356,174 , GRCh38.p12 chrY: 20,297-57,210,023 RPS24P1, CLUHP1, 569 more genes
    nsv3897961copy number variation2nstd102humanPathogenic GRCh37 chrY: 10,701-59,335,913 , GRCh38 chrY: 10,701-57,189,762 , NCBI36 chrY: 701-57,745,301 CSPG4P2Y, LINC00265-2P, 567 more genes
    nsv3909858copy number variation1nstd102humanPathogenic GRCh37 chrY: 288,874-59,327,713 , GRCh38 chrY: 378,139-57,181,562 , NCBI36 chrY: 258,874-57,737,101 RNA5SP498, TSPY4, 563 more genes
    nsv3907887copy number variation1nstd102humanPathogenic NCBI36 chrY: 1,137,123-57,439,959 , GRCh38 chrY: 2,133,003-56,884,424 , GRCh37 chrY: 1,167,123-59,030,571 FAM197Y7, LOC100652931, 533 more genes
    nsv3893244copy number variation1nstd102humanPathogenic GRCh37 chrY: 13,134,518-59,336,737 , NCBI36 chrY: 11,244,518-57,746,125 , GRCh38 chrY: 10,624,004-57,190,586 TTTY4C, LOC105379273, 378 more genes
    nsv3889255copy number variation1nstd102humanPathogenic GRCh37 chrY: 13,410,538-59,032,808 , GRCh38.p12 chrY: 11,254,862-56,886,661 XKRY, RNU6-184P, 360 more genes
    nsv3870660copy number variation1nstd102humanPathogenic GRCh37 chrY: 13,871,147-59,336,737 , GRCh38.p12 chrY: 11,750,441-57,190,586 KDM5D, TTTY3B, 357 more genes
    nsv3923177copy number variation1nstd102humanPathogenic NCBI36 chrY: 12,380,873-57,745,301 , GRCh37.p13 chrY: 13,870,873-59,335,913 , GRCh38.p12 chrY: 11,750,167-57,189,762 TTTY4C, FAM224A, 357 more genes
    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
    nsv3875663copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,698,756-59,031,480 , NCBI36 chrY: 13,208,776-57,440,868 , GRCh38.p12 chrY: 12,586,822-56,885,333 TRIM60P9Y, EIF1AY, 337 more genes
    nsv3900947copy number variation1nstd102humanPathogenic GRCh38 chrY: 12,965,721-57,212,647 , NCBI36 chrY: 13,587,025-57,768,186 , GRCh37 chrY: 15,077,631-59,358,798 KDM5DP1, GAPDHP17, 340 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
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 PSMA6, HNRNPC, 616 more genes
    nsv3873753copy number variation1nstd102humanPathogenic GRCh37 chrY: 168,546-28,451,874 , GRCh38.p12 chrY: 301,879-26,305,727 CDY23P, XKRYP7, 550 more genes
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