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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072267inversion1nstd229human GRCh38 chr8: 66,467,404-66,471,563 , GRCh37.p13 chr8: 67,379,639-67,383,798 ADHFE1
    nsv7066271inversion1nstd229human GRCh38 chr8: 66,464,819-66,490,539 , GRCh37.p13 chr8: 67,377,054-67,402,774 ADHFE1, LOC100131770
    nsv7061527inversion1nstd229human GRCh38 chr8: 66,464,085-66,476,565 , GRCh37.p13 chr8: 67,376,320-67,388,800 ADHFE1
    nsv6855926copy number variation1nstd229human GRCh38 chr8: 66,464,864-66,491,555 , GRCh37.p13 chr8: 67,377,099-67,403,790 LOC100131770, ADHFE1
    nsv6855693copy number variation1nstd229human GRCh38 chr8: 66,415,291-66,476,233 , GRCh37.p13 chr8: 67,327,526-67,388,468 RRS1, ADHFE1, 2 more genes
    nsv6850869copy number variation1nstd229human GRCh38 chr8: 66,440,053-66,442,319 , GRCh37.p13 chr8: 67,352,288-67,354,554 ADHFE1
    nsv6847270copy number variation1nstd229human GRCh38 chr8: 66,437,904-66,443,848 , GRCh37.p13 chr8: 67,350,139-67,356,083 ADHFE1
    nsv6842122copy number variation1nstd229human GRCh38 chr8: 66,459,630-66,465,291 , GRCh37.p13 chr8: 67,371,865-67,377,526 ADHFE1
    nsv6841831copy number variation1nstd229human GRCh38 chr8: 66,438,601-66,441,600 , GRCh37.p13 chr8: 67,350,836-67,353,835 ADHFE1
    nsv6636205copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,261,729-68,676,568 , GRCh38.p12 chr8: 66,349,494-67,764,333 C8orf44-SGK3, SNHG6, 36 more genes
    nsv6561965inversion1nstd223human GRCh38 chr8: 66,441,972-66,442,075 , GRCh37.p13 chr8: 67,354,207-67,354,310 ADHFE1
    nsv6558450inversion1nstd223human GRCh38 chr8: 66,464,085-66,476,565 , GRCh37.p13 chr8: 67,376,320-67,388,800 ADHFE1
    nsv6430517copy number variation1nstd223human GRCh38 chr8: 66,444,712-66,452,292 , GRCh37.p13 chr8: 67,356,947-67,364,527 ADHFE1
    nsv6424976copy number variation1nstd223human GRCh38 chr8: 66,458,501-66,463,700 , GRCh37.p13 chr8: 67,370,736-67,375,935 ADHFE1
    nsv6417304copy number variation1nstd223human GRCh38 chr8: 66,447,249-66,447,768 , GRCh37.p13 chr8: 67,359,484-67,360,003 ADHFE1
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 LINC00967, LOC107986950, 64 more genes
    nsv6136691copy number variation1nstd213human GRCh37 chr8: 67,370,000-67,440,001 , GRCh38.p12 chr8: 66,457,765-66,527,766 ADHFE1, VXN, 2 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv5921571copy number variation1nstd209human GRCh38 chr8: 66,460,796-66,480,798 , GRCh37.p13 chr8: 67,373,031-67,393,033 ADHFE1, LOC100131770
    nsv5854795copy number variation1nstd209human GRCh38 chr8: 66,460,852-66,480,814 , GRCh37.p13 chr8: 67,373,087-67,393,049 ADHFE1, LOC100131770
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