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 317

    loading data ...

    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
    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
    nsv6634185copy number variation1nstd224human GRCh37 chrY: 16,913,677-24,522,333 , GRCh38.p12 chrY: 14,801,797-22,376,186 XKRY, CDY2A, 151 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 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
    nsv6136811copy number variation1nstd213human GRCh37 chrY: 22,510,000-23,960,001 , GRCh38.p12 chrY: 20,348,114-21,813,854 RBMY1A1, RBMY1HP, 30 more genes
    nsv6136810copy number variation1nstd213human GRCh37 chrY: 22,510,000-23,840,001 , GRCh38.p12 chrY: 20,348,114-21,678,115 RBMY1A1, RBMY1HP, 27 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
    nsv5430674copy number variation1nstd206human GRCh38 chrY: 21,375,793-21,531,793 , GRCh37.p13 chrY: 23,537,679-23,693,679 RBMY1HP, RBMY2EP, 4 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
    nsv4728366copy number variation1nstd102humanLikely benign GRCh37 chrY: 23,181,670-23,683,718 , GRCh38.p12 chrY: 21,019,784-21,521,832 RBMY2TP, NEFLP1, 10 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
    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