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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
    nsv6315264copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-7,114,097 , GRCh38.p12 chrY: 2,782,099-7,246,056 RNU6-1334P, SRIP3, 50 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
    nsv6137651copy number variation1nstd213human GRCh37 chrY: 6,130,000-9,230,001 , GRCh38.p12 chrY: 6,261,959-9,392,392 AMELY, PRKY, 82 more genes
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5431206copy number variation1nstd206human GRCh38 chrY: 6,266,388-9,335,488 , GRCh37.p13 chrY: 6,134,429-9,173,097 , RN7SKP282, 76 more genes
    nsv4902832copy number variation1nstd200human GRCh38 chrY: 5,818,577-7,107,701 , GRCh37.p13 chrY: 5,686,618-6,975,742 TSPY17P, AMELY, 21 more genes
    nsv4730219inversion4nstd198human GRCh38 chrY: 6,198,014-9,936,872 , GRCh37.p13 chrY: 6,066,055-9,774,481 , AMELY, 109 more genes
    nsv4728639copy number variation1nstd102humanUncertain significance GRCh37 chrY: 6,148,517-6,818,671 , GRCh38.p12 chrY: 6,280,476-6,950,630 RBMY2GP, ATP5PFP1, 14 more genes
    nsv4684048copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-6,367,818 , GRCh38.p12 chrY: 2,782,099-6,499,777 SNX3P1Y, LOC100533723, 42 more genes
    nsv4684046copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-7,019,586 , GRCh38.p12 chrY: 2,782,099-7,151,545 KRT18P10, TTTY23B, 50 more genes
    nsv4674256copy number variation1nstd102humanLikely benign GRCh37 chrY: 6,152,464-8,586,717 , GRCh38.p12 chrY: 6,284,423-8,718,676 LOC107987339, TTTY21B, 57 more genes
    nsv4674023copy number variation1nstd102humanUncertain significance GRCh37 chrY: 6,135,412-9,155,562 , GRCh38.p12 chrY: 6,267,371-9,317,953 MTND2P3, TBL1Y, 73 more genes
    nsv4674007copy number variation1nstd102humanLikely benign GRCh37 chrY: 6,172,777-9,168,128 , GRCh38.p12 chrY: 6,304,736-9,330,519 TSPY12P, GOT2P5, 74 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
    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
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