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Items: 1 to 20 of 343

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    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
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