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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
    nsv6636023copy number variation1nstd102humanUncertain significance GRCh37 chrY: 24,644,461-28,341,390 , GRCh38.p12 chrY: 22,498,314-26,195,243 LOC107987349, RNU1-97P, 146 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
    nsv6634342copy number variation1nstd102humanUncertain significance GRCh37 chrY: 25,856,644-27,811,846 , GRCh38.p12 chrY: 23,710,497-25,665,699 XKRYP3, UBE2Q2P5Y, 84 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315369copy number variation1nstd102humanUncertain significance GRCh37 chrY: 25,856,867-28,113,239 , GRCh38.p12 chrY: 23,710,720-25,967,092 ZNF736P4Y, CSPG4P3Y, 104 more genes
    nsv6315362copy number variation1nstd102humanUncertain significance GRCh37 chrY: 24,985,375-28,458,663 , GRCh38.p12 chrY: 22,839,228-26,312,516 DAZ4, UBE2Q2P4Y, 136 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
    nsv6290621copy number variation1nstd102humanUncertain significance GRCh37 chrY: 24,770,885-28,410,810 , GRCh38.p12 chrY: 22,624,738-26,264,663 DNM1P27, ZNF736P12Y, 139 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
    nsv4728497copy number variation1nstd102humanUncertain significance GRCh37 chrY: 25,403,868-27,224,389 , GRCh38.p12 chrY: 23,257,721-25,078,242 RBMY2CP, ELOCP16, 70 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
    nsv4684045copy number variation1nstd102humanPathogenic GRCh37 chrY: 24,644,460-28,341,390 , GRCh38.p12 chrY: 22,498,313-26,195,243 USP9YP35, ZNF736P12Y, 146 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
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