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Items: 1 to 20 of 315

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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
    nsv5423876copy number variation1nstd206human GRCh38 chrY: 9,108,931-21,750,314 , GRCh37.p13 chrY: 8,964,956-23,901,428 , TSPY14P, 238 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
    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
    nsv4684020copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,495,040-24,070,172 , GRCh38.p12 chrY: 12,383,237-21,924,025 TMEM167AP1, ELOCP13, 157 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
    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
    nsv4674460copy number variation1nstd102humanUncertain significance GRCh37 chrY: 23,553,019-23,841,524 , GRCh38.p12 chrY: 21,391,133-21,679,638 RBMY1HP, RBMY2TP, 10 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
    nsv4518166copy number variation1nstd166human GRCh37.p13 chrY: 20,611,898-24,225,000 , GRCh38.p12 chrY: 18,450,012-22,078,853 RPS4Y2, TXLNGY, 80 more genes
    nsv4517121copy number variation1nstd166human GRCh37.p13 chrY: 23,718,999-23,901,428 , GRCh38.p12 chrY: 21,557,113-21,739,542 , GRCh38.p12 chrY|NW_018654726.1: 1-160,601 RBMY1A1, TTTY13, 5 more genes
    nsv4516671copy number variation1nstd166human GRCh37.p13 chrY: 23,757,799-24,213,700 , GRCh38.p12 chrY: 21,595,913-22,067,553 RBMY1E, RBMY2AP, 15 more genes
    nsv4453832copy number variation1nstd102humanPathogenic GRCh37 chrY: 21,039,792-28,799,937 , GRCh38.p12 chrY: 18,877,906-26,653,790 EIF1AY, TRIM60P11Y, 228 more genes
    nsv4452235copy number variation1nstd102humanPathogenic GRCh37 chrY: 21,035,530-59,336,737 , GRCh38.p12 chrY: 18,873,644-57,190,586 CDY14P, RNU1-40P, 236 more genes
    nsv4451941copy number variation1nstd102humanPathogenic GRCh37 chrY: 16,053,146-59,343,488 , GRCh38.p12 chrY: 13,941,266-57,197,337 CD24P4, CSPG4P1Y, 327 more genes
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