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Items: 1 to 20 of 313

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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
    nsv5432002copy number variation1nstd206human GRCh38 chrY: 17,451,387-18,881,388 , GRCh37.p13 chrY: 19,563,267-21,043,274 ACTG1P2, RNU1-95P, 75 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
    nsv4730265inversion3nstd198human GRCh38 chrY: 17,951,224-18,012,034 , GRCh37.p13 chrY: 20,063,104-20,123,914 CDY7P, USP9YP34, 1 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
    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
    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
    nsv4674670copy number variation1nstd102humanLikely benign GRCh37 chrY: 19,471,085-20,603,124 , GRCh38.p12 chrY: 17,359,205-18,441,238 ELOCP6, XKRYP7, 48 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
    nsv4517475copy number variation1nstd166human GRCh37.p13 chrY: 19,912,899-20,303,200 , GRCh38.p12 chrY: 17,801,019-18,141,314 CDY8P, USP9YP6, 17 more genes
    nsv4516790copy number variation1nstd166human GRCh37.p13 chrY: 19,505,051-20,810,338 , GRCh38.p12 chrY: 17,393,171-18,648,452 CDY7P, RNA5SP522, 61 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
    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
    nsv4451757copy number variation1nstd102humanPathogenic GRCh37 chrY: 15,190,336-59,343,488 , GRCh38.p12 chrY: 13,078,422-57,197,337 DPH3P2, CDY16P, 337 more genes
    nsv4385524copy number variation3nstd173human GRCh37 chrY: 2,650,141-28,799,949 , GRCh38.p12 chrY: 2,782,100-26,653,802 , MTND1P12, 527 more genes
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