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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634344copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-9,651,417 , GRCh38.p12 chrY: 2,782,099-9,813,808 LOC105377235, TTTY7B, 135 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
    nsv6293773copy number variation1nstd186human GRCh37 chrY: 9,639,322-9,651,322 , GRCh38.p12 chrY: 9,801,713-9,813,713 TTTY22
    nsv6139079copy number variation1nstd206human GRCh38 chrY: 9,801,713-9,813,713 , GRCh37.p13 chrY: 9,639,322-9,651,322 TTTY22
    nsv6137423copy number variation1nstd213human GRCh37 chrY: 9,370,000-10,090,001 , GRCh38.p12 chrY: 9,532,391-10,252,392 TTTY1, TTTY2, 26 more genes
    nsv6137422copy number variation1nstd213human GRCh37 chrY: 9,360,000-10,080,001 , GRCh38.p12 chrY: 9,522,391-10,242,392 TTTY1, TTTY2, 28 more genes
    nsv6137421copy number variation1nstd213human GRCh37 chrY: 9,360,000-10,000,001 , GRCh38.p12 chrY: 9,522,391-10,162,392 TTTY1, TTTY2, 22 more genes
    nsv6137240copy number variation2nstd213human GRCh37 chrY: 9,360,000-10,100,001 , GRCh38.p12 chrY: 9,522,391-10,262,392 TTTY1, TTTY2, 28 more genes
    nsv6114371copy number variation1nstd186human GRCh37 chrY: 9,639,997-9,650,928 , GRCh38.p12 chrY: 9,802,388-9,813,319 TTTY22
    nsv5969627copy number variation2nstd209human GRCh38 chrY: 9,800,811-9,816,019 , GRCh37.p13 chrY: 9,638,420-9,653,628 TTTY22
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5432395copy number variation1nstd206human GRCh38 chrY: 9,789,088-10,213,388 , GRCh37.p13 chrY: 9,626,697-10,050,997 RNA5SP518, TSPY18P, 17 more genes
    nsv5431730copy number variation1nstd206human GRCh38 chrY: 9,802,388-9,813,319 , GRCh37.p13 chrY: 9,639,997-9,650,928 TTTY22
    nsv5423876copy number variation1nstd206human GRCh38 chrY: 9,108,931-21,750,314 , GRCh37.p13 chrY: 8,964,956-23,901,428 , TSPY14P, 238 more genes
    nsv4730219inversion4nstd198human GRCh38 chrY: 6,198,014-9,936,872 , GRCh37.p13 chrY: 6,066,055-9,774,481 , AMELY, 109 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
    nsv4635558copy number variation1nstd186human GRCh37 chrY: 9,640,000-9,650,350 , GRCh38.p12 chrY: 9,802,391-9,812,741 TTTY22
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