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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097765copy number variation1nstd102humanUncertain significance GRCh37 chr7: 96,318,236-97,493,828 , GRCh38.p12 chr7: 96,688,924-97,864,516 RN7SKP104, CZ1P-ASNS, 16 more genes
    nsv7056087inversion1nstd229human GRCh38 chr7: 97,153,617-97,157,062 , GRCh37.p13 chr7: 96,782,929-96,786,374 LOC107984034, SDHAF3
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv6835375copy number variation1nstd229human GRCh38 chr7: 97,144,444-97,160,702 , GRCh37.p13 chr7: 96,773,756-96,790,014 SDHAF3, LOC107984034
    nsv6832864copy number variation1nstd229human GRCh38 chr7: 97,151,035-97,155,477 , GRCh37.p13 chr7: 96,780,347-96,784,789 LOC107984034, SDHAF3
    nsv6832801copy number variation1nstd229human GRCh38 chr7: 97,153,767-97,162,260 , GRCh37.p13 chr7: 96,783,079-96,791,572 SDHAF3, LOC107984034
    nsv6832147copy number variation1nstd229human GRCh38 chr7: 97,109,801-97,115,900 , GRCh37.p13 chr7: 96,739,113-96,745,212 SDHAF3
    nsv6830268copy number variation1nstd229human GRCh38 chr7: 97,160,091-97,163,551 , GRCh37.p13 chr7: 96,789,403-96,792,863 SDHAF3
    nsv6830158copy number variation1nstd229human GRCh38 chr7: 97,162,842-97,162,883 , GRCh37.p13 chr7: 96,792,154-96,792,195 SDHAF3
    nsv6828925copy number variation1nstd229human GRCh38 chr7: 97,128,640-97,129,399 , GRCh37.p13 chr7: 96,757,952-96,758,711 SDHAF3
    nsv6824578copy number variation1nstd229human GRCh38 chr7: 97,117,327-97,132,049 , GRCh37.p13 chr7: 96,746,639-96,761,361 SDHAF3
    nsv6819098copy number variation1nstd229human GRCh38 chr7: 97,132,401-97,132,543 , GRCh37.p13 chr7: 96,761,713-96,761,855 SDHAF3
    nsv6636511copy number variation1nstd102humanPathogenic GRCh37 chr7: 96,264,152-96,860,892 , GRCh38.p12 chr7: 96,634,840-97,231,580 SDHAF3, DLX6, 9 more genes
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6616578copy number variation1nstd223human GRCh38 chr7: 97,160,091-97,163,548 , GRCh37.p13 chr7: 96,789,403-96,792,860 SDHAF3
    nsv6614030copy number variation1nstd223human GRCh38 chr7: 97,151,035-97,155,477 , GRCh37.p13 chr7: 96,780,347-96,784,789 SDHAF3, LOC107984034
    nsv6613624copy number variation1nstd223human GRCh38 chr7: 97,117,714-97,118,150 , GRCh37.p13 chr7: 96,747,026-96,747,462 SDHAF3
    nsv6560817inversion1nstd223human GRCh38 chr7: 97,145,478-97,146,733 , GRCh37.p13 chr7: 96,774,790-96,776,045 SDHAF3, LOC107984034
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