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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636160copy number variation1nstd102humanUncertain significance GRCh37 chrY: 24,137,684-25,844,774 , GRCh38.p12 chrY: 21,991,537-23,698,627 RBMY1F, RBMY1J, 54 more genes
    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
    nsv6635999copy number variation1nstd102humanUncertain significance GRCh37 chrY: 24,103,932-24,892,425 , GRCh38.p12 chrY: 21,957,785-22,746,278 USP9YP24, HSFY5P, 30 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
    nsv6138450copy number variation1nstd206human GRCh38 chrY: 21,926,984-26,551,584 , GRCh37.p13 chrY: 24,073,131-28,697,731 , UBE2Q2P5Y, 177 more genes
    nsv6127496insertion1nstd186human GRCh37 chrY: 13,193,955-58,979,440 , GRCh38.p12 chrY: 11,038,279-56,833,293 , ELOCP10, 371 more genes
    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
    nsv5423602copy number variation1nstd206human GRCh38 chrY: 22,020,088-22,557,281 , GRCh37.p13 chrY: 24,166,235-24,703,428 LOC101929148, TTTY5, 26 more genes
    nsv5421434copy number variation1nstd206human GRCh38 chrY: 21,913,281-22,563,281 , GRCh37.p13 chrY: 24,059,428-24,709,428 RBMY2VP, RBMY1E, 29 more genes
    nsv4730228inversion2nstd198human GRCh38 chrY: 21,899,633-22,637,147 , GRCh37.p13 chrY: 24,045,780-24,783,294 RBMY2AP, PRY, 31 more genes
    nsv4684203copy number variation1nstd102humanLikely pathogenic GRCh37 chrY: 24,007,925-24,891,486 , GRCh38.p12 chrY: 21,861,778-22,745,339 RBMY2AP, PRY, 33 more genes
    nsv4684052copy number variation1nstd102humanPathogenic GRCh37 chrY: 21,719,615-28,799,937 , GRCh38.p12 chrY: 19,557,729-26,653,790 PRY, RBMY2BP, 221 more genes
    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
    nsv4684042copy number variation1nstd102humanPathogenic GRCh37 chrY: 18,546,605-28,799,937 , GRCh38.p12 chrY: 16,434,725-26,653,790 ANKRD36P1, LOC105377217, 305 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
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