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Items: 1 to 20 of 332

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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
    nsv6777013copy number variation1nstd229human GRCh38 chr5: 79,679,014-79,679,147 , GRCh37.p13 chr5: 78,974,837-78,974,970 TENT2
    nsv6776039copy number variation1nstd229human GRCh38 chr5: 79,657,463-79,664,096 , GRCh37.p13 chr5: 78,953,286-78,959,919 TENT2
    nsv6769263copy number variation1nstd229human GRCh38 chr5: 79,583,656-79,657,825 , GRCh37.p13 chr5: 78,879,479-78,953,648 TENT2
    nsv6766588copy number variation1nstd229human GRCh38 chr5: 79,593,810-79,616,090 , GRCh37.p13 chr5: 78,889,633-78,911,913 TENT2
    nsv6763728copy number variation1nstd229human GRCh38 chr5: 79,657,401-79,665,700 , GRCh37.p13 chr5: 78,953,224-78,961,523 TENT2
    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
    nsv6760402copy number variation1nstd229human GRCh38 chr5: 79,621,301-79,622,900 , GRCh37.p13 chr5: 78,917,124-78,918,723 TENT2
    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
    nsv6572213inversion1nstd223human GRCh38 chr5: 79,669,947-79,670,493 , GRCh37.p13 chr5: 78,965,770-78,966,316 TENT2
    nsv6571972inversion1nstd223human GRCh38 chr5: 79,671,600-79,671,861 , GRCh37.p13 chr5: 78,967,423-78,967,684 TENT2
    nsv6563712inversion1nstd223human GRCh38 chr5: 79,633,547-79,634,148 , GRCh37.p13 chr5: 78,929,370-78,929,971 TENT2
    nsv6562647inversion1nstd223human GRCh38 chr5: 79,626,427-79,626,854 , GRCh37.p13 chr5: 78,922,250-78,922,677 TENT2
    nsv6413303copy number variation1nstd223human GRCh38 chr5: 79,614,384-79,616,396 , GRCh37.p13 chr5: 78,910,207-78,912,219 TENT2
    nsv6412621copy number variation1nstd223human GRCh38 chr5: 79,642,201-79,643,500 , GRCh37.p13 chr5: 78,938,024-78,939,323 TENT2
    nsv6412192copy number variation1nstd223human GRCh38 chr5: 79,655,049-79,655,414 , GRCh37.p13 chr5: 78,950,872-78,951,237 TENT2
    nsv6410327copy number variation1nstd223human GRCh38 chr5: 79,626,885-79,629,887 , GRCh37.p13 chr5: 78,922,708-78,925,710 TENT2
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