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Items: 1 to 20 of 347

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636057copy number variation1nstd102humanUncertain significance GRCh37 chrY: 16,203,971-59,336,737 , GRCh38.p12 chrY: 14,092,091-57,190,586 RBMY2YP, FAM8A9P, 324 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
    nsv6634185copy number variation1nstd224human GRCh37 chrY: 16,913,677-24,522,333 , GRCh38.p12 chrY: 14,801,797-22,376,186 XKRY, CDY2A, 151 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
    nsv6138184copy number variation1nstd206human GRCh38 chrY: 19,047,824-19,498,360 , GRCh37.p13 chrY: 21,209,710-21,660,246 GAPDHP19, LOC102723934, 2 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
    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
    nsv6136808copy number variation1nstd213human GRCh37 chrY: 20,550,000-22,230,001 , GRCh38.p12 chrY: 18,388,114-20,068,115 CD24P4, KDM5D, 40 more genes
    nsv6127496insertion1nstd186human GRCh37 chrY: 13,193,955-58,979,440 , GRCh38.p12 chrY: 11,038,279-56,833,293 , ELOCP10, 371 more genes
    nsv5974027copy number variation1nstd209human GRCh38 chrY: 19,486,920-19,488,819 , GRCh37.p13 chrY: 21,648,806-21,650,705 BCORP1
    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
    nsv5174502mobile element insertion1nstd203human GRCh38 chrY: 19,463,914-19,463,930 , GRCh37.p13 chrY: 21,625,800-21,625,816 BCORP1
    nsv4902946copy number variation1nstd200human GRCh38 chrY: 19,457,208-19,459,890 , GRCh37.p13 chrY: 21,619,094-21,621,776 BCORP1
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