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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv4684037copy number variation1nstd102humanPathogenic GRCh37 chrY: 24,770,884-28,355,431 , GRCh38.p12 chrY: 22,624,737-26,209,284 TRAPPC2P4, ZNF736P2Y, 139 more genes
    nsv4684035copy number variation1nstd102humanPathogenic GRCh37 chrY: 20,111,978-28,423,925 , GRCh38.p12 chrY: 18,000,098-26,277,778 SEPTIN14P23, RNU1-107P, 267 more genes
    nsv4684031copy number variation1nstd102humanPathogenic GRCh37 chrY: 24,651,462-28,328,263 , GRCh38.p12 chrY: 22,505,315-26,182,116 HSFY6P, LOC105377238, 145 more genes
    nsv4684028copy number variation1nstd102humanPathogenic GRCh37 chrY: 23,887,108-28,799,937 , GRCh38.p12 chrY: 21,725,222-26,653,790 TTTY6B, RNU1-107P, 185 more genes
    nsv4684018copy number variation1nstd102humanPathogenic GRCh37 chrY: 20,608,554-28,799,937 , GRCh38.p12 chrY: 18,446,668-26,653,790 ZNF736P11Y, OFD1P14Y, 254 more genes
    nsv4674736copy number variation1nstd102humanPathogenic GRCh37 chrY: 24,770,884-59,336,737 , GRCh38.p12 chrY: 22,624,737-57,190,586 HSFY6P, RAB9AP5, 157 more genes
    nsv4674682copy number variation1nstd102humanLikely benign GRCh37 chrY: 19,567,361-28,458,663 , GRCh38.p12 chrY: 17,455,481-26,312,516 ELOCP13, OFD1P5Y, 295 more genes
    nsv4674190copy number variation1nstd102humanPathogenic GRCh37 chrY: 26,241,299-59,336,737 , GRCh38.p12 chrY: 24,095,152-57,190,586 DNM1P27, RNU6-1314P, 107 more genes
    nsv4674153copy number variation1nstd102humanLikely benign GRCh37 chrY: 24,644,460-28,423,925 , GRCh38.p12 chrY: 22,498,313-26,277,778 CSPG4P2Y, ELOCP34, 147 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
    nsv4650448copy number variation1nstd186human GRCh37 chrY: 28,053,000-28,104,000 , GRCh38.p12 chrY: 25,906,853-25,957,853 TRAPPC2P4, XKRYP6, 4 more genes
    nsv4640234copy number variation1nstd186human GRCh37 chrY: 27,868,250-28,076,800 , GRCh38.p12 chrY: 25,722,103-25,930,653 OFD1P14Y, XKRYP5, 13 more genes
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