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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891899copy number variation1nstd209human GRCh38 chr5: 160,047,152-160,047,740 , GRCh37.p13 chr5: 159,474,159-159,474,747 PWWP2A, TTC1
    nsv5727115mobile element insertion2nstd211human GRCh38 chr5: 160,021,499-160,021,499 , GRCh37.p13 chr5: 159,448,506-159,448,506 TTC1
    nsv5718226mobile element insertion1nstd211human GRCh38 chr5: 160,057,436-160,057,436 , GRCh37.p13 chr5: 159,484,443-159,484,443 TTC1, PWWP2A
    nsv5688120mobile element insertion1nstd211human GRCh38 chr5: 160,064,844-160,064,844 , GRCh37.p13 chr5: 159,491,851-159,491,851 PWWP2A, TTC1
    nsv5560464mobile element insertion1nstd206human GRCh38 chr5: 160,021,511-160,021,550 , GRCh37.p13 chr5: 159,448,518-159,448,557 TTC1
    nsv5472099copy number variation1nstd206human GRCh38 chr5: 160,047,153-160,047,741 , GRCh37.p13 chr5: 159,474,160-159,474,748 TTC1, PWWP2A
    nsv5471690copy number variation1nstd206human GRCh38 chr5: 160,052,240-160,052,348 , GRCh37.p13 chr5: 159,479,247-159,479,355 TTC1, PWWP2A
    nsv5460186copy number variation1nstd206human GRCh38 chr5: 160,061,289-160,082,089 , GRCh37.p13 chr5: 159,488,296-159,509,096 TTC1, PWWP2A
    nsv5457398copy number variation1nstd206human GRCh38 chr5: 160,051,058-160,051,127 , GRCh37.p13 chr5: 159,478,065-159,478,134 TTC1, PWWP2A
    nsv5409218mobile element insertion1nstd206human GRCh38 chr5: 160,064,844-160,064,895 , GRCh37.p13 chr5: 159,491,851-159,491,902 PWWP2A, TTC1
    nsv5362608translocation1nstd200human GRCh38 chr5: 160,047,153-160,047,153 , GRCh38 chr5: 160,047,741-160,047,741 , GRCh37.p13 chr5: 159,474,160-159,474,160 , GRCh37.p13 chr5: 159,474,748-159,474,748 PWWP2A, TTC1
    nsv5314037copy number variation1nstd204human GRCh38.p13 chr5: 160,061,299-160,082,078 , GRCh37.p13 chr5: 159,488,306-159,509,085 TTC1, PWWP2A
    nsv5312256copy number variation1nstd204human GRCh37.p13 chr5: 159,474,157-159,474,749 , GRCh38.p13 chr5: 160,047,150-160,047,742 PWWP2A, TTC1
    nsv5238035copy number variation1nstd204human GRCh38.p13 chr5: 160,061,230-160,078,405 , GRCh37.p13 chr5: 159,488,237-159,505,412 PWWP2A, TTC1
    nsv5193032mobile element insertion1nstd203human GRCh38 chr5: 160,057,421-160,057,436 , GRCh37.p13 chr5: 159,484,428-159,484,443 TTC1, PWWP2A
    nsv5187581mobile element insertion1nstd203human GRCh38 chr5: 160,057,436-160,057,436 , GRCh37.p13 chr5: 159,484,443-159,484,443 TTC1, PWWP2A
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4949137copy number variation1nstd200human GRCh38 chr5: 160,061,308-160,082,070 , GRCh37.p13 chr5: 159,488,315-159,509,077 PWWP2A, TTC1
    nsv4949136copy number variation1nstd200human GRCh38 chr5: 160,032,672-160,038,766 , GRCh37.p13 chr5: 159,459,679-159,465,773 TTC1
    nsv4949135copy number variation1nstd200human GRCh38 chr5: 160,010,131-160,014,353 , GRCh37.p13 chr5: 159,437,138-159,441,360 TTC1
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