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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050546inversion1nstd229human GRCh38 chr5: 79,227,383-80,480,748 , GRCh37.p13 chr5: 78,523,206-79,776,567 TENT2, SPZ1, 27 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv6763423copy number variation1nstd229human GRCh38 chr5: 77,899,127-80,222,849 , GRCh37.p13 chr5: 77,194,951-79,518,668 RNU6-183P, ARSB, 34 more genes
    nsv6763261copy number variation1nstd229human GRCh38 chr5: 79,244,881-79,631,540 , GRCh37.p13 chr5: 78,540,704-78,927,363 JMY, HOMER1, 8 more genes
    nsv6762857copy number variation1nstd229human GRCh38 chr5: 79,367,109-79,903,818 , GRCh37.p13 chr5: 78,662,932-79,199,641 LOC101929201, CMYA5, 8 more genes
    nsv6636260copy number variation1nstd102humanUncertain significance GRCh37 chr5: 77,746,948-79,089,197 , GRCh38.p12 chr5: 78,451,125-79,793,374 RPL29P15, LOC102724530, 18 more genes
    nsv6296590copy number variation1nstd186human GRCh37 chr5: 78,798,534-78,913,255 , GRCh38.p12 chr5: 79,502,711-79,617,432 HOMER1, RPL7AP32, 3 more genes
    nsv6135683copy number variation1nstd213human GRCh37 chr5: 76,940,000-80,890,001 , GRCh38.p12 chr5: 77,644,175-81,594,182 ACTBP2, ARSB, 63 more genes
    nsv6135437copy number variation1nstd213human GRCh37 chr5: 78,580,000-80,500,001 , GRCh38.p12 chr5: 79,284,177-81,204,182 DBIP2, DHFR, 40 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5461569copy number variation1nstd206human GRCh38 chr5: 79,502,711-79,617,432 , GRCh37.p13 chr5: 78,798,534-78,913,255 HOMER1, RPL7AP32, 3 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4805612copy number variation1nstd200human GRCh37 chr5: 78,798,534-78,913,255 , GRCh38.p12 chr5: 79,502,711-79,617,432 RPL29P15, TENT2, 3 more genes
    nsv4675682copy number variation1nstd102humanUncertain significance GRCh37 chr5: 78,094,810-78,936,391 , GRCh38.p12 chr5: 78,798,987-79,640,568 LOC107986426, ARSB, 14 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4456838copy number variation1nstd102humanUncertain significance GRCh37 chr5: 78,229,182-78,844,914 , GRCh38.p12 chr5: 78,933,359-79,549,091 BHMT2, LOC102724530, 13 more genes
    nsv4456095copy number variation1nstd102humanUncertain significance GRCh37 chr5: 78,687,874-79,208,782 , GRCh38.p12 chr5: 79,392,051-79,912,959 CMYA5, LOC107986426, 7 more genes
    nsv4455617copy number variation1nstd102humanUncertain significance GRCh37 chr5: 78,700,197-79,294,390 , GRCh38.p12 chr5: 79,404,374-79,998,567 LOC102724557, THBS4, 10 more genes
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