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Items: 1 to 20 of 576

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978449copy number variation1nstd209human GRCh38 chrY: 5,101,759-5,107,532 , GRCh37.p13 chrY: 4,969,800-4,975,573 PCDH11Y
    nsv5977269copy number variation1nstd209human GRCh38 chrY: 5,357,348-5,373,374 , GRCh37.p13 chrY: 5,225,389-5,241,415 PCDH11Y
    nsv5972927copy number variation1nstd209human GRCh38 chrY: 5,101,394-5,112,367 , GRCh37.p13 chrY: 4,969,435-4,980,408 PCDH11Y
    nsv5723197mobile element insertion1nstd211human GRCh38 chrY: 5,027,408-5,027,408 , GRCh37.p13 chrY: 4,895,449-4,895,449 PCDH11Y
    nsv5671890copy number variation1nstd207human GRCh38 chrY: 5,348,007-5,348,076 , GRCh37.p13 chrY: 5,216,048-5,216,117 PCDH11Y
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5671274copy number variation1nstd207human GRCh38 chrY: 5,092,130-5,092,179 , GRCh37.p13 chrY: 4,960,171-4,960,220 PCDH11Y
    nsv5669850copy number variation1nstd207human GRCh38 chrY: 5,311,482-5,311,535 , GRCh37.p13 chrY: 5,179,523-5,179,576 PCDH11Y
    nsv5669653copy number variation1nstd207human GRCh38 chrY: 5,107,772-5,108,097 , GRCh37.p13 chrY: 4,975,813-4,976,138 PCDH11Y
    nsv5669646copy number variation1nstd207human GRCh38 chrY: 5,115,736-5,116,050 , GRCh37.p13 chrY: 4,983,777-4,984,091 PCDH11Y
    nsv5667846copy number variation1nstd207human GRCh38 chrY: 5,140,830-5,142,254 , GRCh37.p13 chrY: 5,008,871-5,010,295 PCDH11Y
    nsv5666001copy number variation1nstd207human GRCh38 chrY: 5,004,801-5,004,890 , GRCh37.p13 chrY: 4,872,842-4,872,931 PCDH11Y
    nsv5619868insertion1nstd207human GRCh38 chrY: 5,314,646-5,314,646 , GRCh37.p13 chrY: 5,182,687-5,182,687 PCDH11Y
    nsv5615420insertion1nstd207human GRCh38 chrY: 5,373,126-5,373,126 , GRCh37.p13 chrY: 5,241,167-5,241,167 PCDH11Y
    nsv5607900insertion1nstd207human GRCh38 chrY: 5,525,239-5,525,239 , GRCh37.p13 chrY: 5,393,280-5,393,280 PCDH11Y
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5549696insertion1nstd206human GRCh38 chrY: 5,334,627-5,334,665 , GRCh37.p13 chrY: 5,202,668-5,202,706 PCDH11Y
    nsv5426994copy number variation1nstd206human GRCh38 chrY: 5,104,604-5,109,134 , GRCh37.p13 chrY: 4,972,645-4,977,175 PCDH11Y
    nsv5422903copy number variation1nstd206human GRCh38 chrY: 5,154,889-5,154,969 , GRCh37.p13 chrY: 5,022,930-5,023,010 PCDH11Y
    nsv5417766copy number variation1nstd206human GRCh38 chrY: 5,107,661-5,109,217 , GRCh37.p13 chrY: 4,975,702-4,977,258 PCDH11Y
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