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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097159copy number variation2nstd102humanUncertain significance GRCh37 chr5: 73,980,960-75,008,762 , GRCh38.p12 chr5: 74,685,135-75,712,937 NSA2, RNU6-680P, 22 more genes
    nsv7055604inversion1nstd229human GRCh38 chr5: 75,187,257-75,187,342 , GRCh37.p13 chr5: 74,483,082-74,483,167 ANKRD31
    nsv7049027inversion1nstd229human GRCh38 chr5: 75,117,751-75,202,611 , GRCh37.p13 chr5: 74,413,576-74,498,436 ANKRD31
    nsv7045293inversion1nstd229human GRCh38 chr5: 73,247,847-76,069,477 , GRCh37.p13 chr5: 72,543,674-75,365,302 LOC107986423, NSA2, 48 more genes
    nsv7043454inversion1nstd229human GRCh38 chr5: 75,201,212-75,286,614 , GRCh37.p13 chr5: 74,497,037-74,582,439 ANKRD31, SUMO2P5
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv7039450inversion1nstd229human GRCh38 chr5: 75,101,117-75,132,930 , GRCh37.p13 chr5: 74,396,942-74,428,755 ANKRD31
    nsv6777892copy number variation1nstd229human GRCh38 chr5: 75,095,580-75,104,431 , GRCh37.p13 chr5: 74,391,405-74,400,256 ANKRD31
    nsv6777556copy number variation1nstd229human GRCh38 chr5: 75,087,170-75,087,340 , GRCh37.p13 chr5: 74,382,995-74,383,165 ANKRD31
    nsv6777103copy number variation1nstd229human GRCh38 chr5: 75,076,518-75,226,932 , GRCh37.p13 chr5: 74,372,343-74,522,757 SUMO2P5, ANKRD31
    nsv6775756copy number variation1nstd229human GRCh38 chr5: 75,028,001-75,106,000 , GRCh37.p13 chr5: 74,323,826-74,401,825 GCNT4, ANKRD31
    nsv6773847copy number variation1nstd229human GRCh38 chr5: 75,178,522-75,182,530 , GRCh37.p13 chr5: 74,474,347-74,478,355 ANKRD31
    nsv6772942copy number variation1nstd229human GRCh38 chr5: 75,182,101-75,182,294 , GRCh37.p13 chr5: 74,477,926-74,478,119 ANKRD31
    nsv6772584copy number variation1nstd229human GRCh38 chr5: 75,236,537-75,238,012 , GRCh37.p13 chr5: 74,532,362-74,533,837 ANKRD31
    nsv6770536copy number variation1nstd229human GRCh38 chr5: 75,192,043-75,209,725 , GRCh37.p13 chr5: 74,487,868-74,505,550 ANKRD31
    nsv6768239copy number variation1nstd229human GRCh38 chr5: 75,184,108-75,188,730 , GRCh37.p13 chr5: 74,479,933-74,484,555 ANKRD31
    nsv6768054copy number variation1nstd229human GRCh38 chr5: 75,079,101-75,089,600 , GRCh37.p13 chr5: 74,374,926-74,385,425 ANKRD31
    nsv6766358copy number variation1nstd229human GRCh38 chr5: 75,014,940-75,480,448 , GRCh37.p13 chr5: 74,310,765-74,776,273 ANKRD31, GCNT4, 4 more genes
    nsv6765392copy number variation1nstd229human GRCh38 chr5: 75,073,275-75,073,347 , GRCh37.p13 chr5: 74,369,100-74,369,172 ANKRD31
    nsv6764028copy number variation1nstd229human GRCh38 chr5: 75,172,526-75,177,008 , GRCh37.p13 chr5: 74,468,351-74,472,833 ANKRD31
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