U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 349

    loading data ...

    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
    nsv5423792copy number variation1nstd206human GRCh38 chrY: 22,207,834-22,323,613 , GRCh37.p13 chrY: 24,353,981-24,469,760 TTTY5, RBMY2FP, 3 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
    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
    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
    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
    nsv4673949copy number variation1nstd102humanPathogenic GRCh37 chrY: 168,546-28,799,937 , GRCh38.p12 chrY: 301,879-26,653,790 GPM6BP2, TTTY18, 559 more genes
    nsv4518340copy number variation1nstd166human GRCh37.p13 chrY: 24,435,699-25,505,000 , GRCh38.p12 chrY: 22,289,552-23,358,853 TTTY5, RBMY2BP, 31 more genes
    nsv4517671copy number variation1nstd166human GRCh37.p13 chrY: 24,227,999-24,470,000 , GRCh38.p12 chrY: 22,081,852-22,323,853 TTTY5, RBMY1F, 9 more genes
    nsv4516894copy number variation1nstd166human GRCh37.p13 chrY: 24,238,599-24,640,600 , GRCh38.p12 chrY: 22,092,452-22,494,453 RBMY1KP, RBMY2VP, 16 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center