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Items: 1 to 20 of 260

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074449inversion1nstd229human GRCh38 chr10: 79,521,421-80,234,809 , GRCh37.p13 chr10: 81,281,177-81,994,565 LINC02679, LOC642361, 29 more genes
    nsv7070338inversion1nstd229human GRCh38 chr10: 79,538,419-80,221,732 , GRCh37.p13 chr10: 81,298,175-81,981,488 RPL22P18, BEND3P3, 29 more genes
    nsv7067530inversion1nstd229human GRCh38 chr10: 79,527,707-80,210,201 , GRCh37.p13 chr10: 81,287,463-81,969,957 PGGT1BP2, ZNRF2P3, 28 more genes
    nsv7067361inversion1nstd229human GRCh38 chr10: 78,238,187-80,195,843 , GRCh37.p13 chr10: 79,997,944-81,955,599 SFTPA3P, MBL3P, 42 more genes
    nsv7066359inversion1nstd229human GRCh38 chr10: 79,541,399-80,221,640 , GRCh37.p13 chr10: 81,301,155-81,981,396 SFTPA3P, MBL3P, 29 more genes
    nsv7063158inversion1nstd229human GRCh38 chr10: 80,046,767-80,101,831 , GRCh37.p13 chr10: 81,806,523-81,861,587 TMEM254-AS1, TMEM254
    nsv7062550inversion1nstd229human GRCh38 chr10: 79,490,527-80,122,745 , GRCh37.p13 chr10: 81,250,283-81,882,501 NUTM2B-AS1, LOC100421010, 27 more genes
    nsv6896866copy number variation1nstd229human GRCh38 chr10: 80,091,600-80,388,756 , GRCh37.p13 chr10: 81,851,356-82,148,512 LINC00857, EIF5AP4, 10 more genes
    nsv6893720copy number variation1nstd229human GRCh38 chr10: 76,896,077-84,570,412 , GRCh37.p13 chr10: 78,655,835-86,330,168 RNU6-129P, LOC105378392, 111 more genes
    nsv6888885copy number variation1nstd229human GRCh38 chr10: 79,983,980-80,080,285 , GRCh37.p13 chr10: 81,743,736-81,840,041 TMEM254-AS1, C1DP4, 3 more genes
    nsv6888482copy number variation1nstd229human GRCh38 chr10: 80,060,210-80,089,847 , GRCh37.p13 chr10: 81,819,966-81,849,603 TMEM254, TMEM254-AS1
    nsv6887772copy number variation1nstd229human GRCh38 chr10: 80,087,055-80,089,055 , GRCh37.p13 chr10: 81,846,811-81,848,811 TMEM254
    nsv6881727copy number variation1nstd229human GRCh38 chr10: 80,087,398-80,158,307 , GRCh37.p13 chr10: 81,847,154-81,918,063 TMEM254, ANXA11, 2 more genes
    nsv6638011copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,603,170-81,984,775 , GRCh38.p12 chr10: 79,843,414-80,225,019 DPY19L2P5, CTSLP6, 18 more genes
    nsv6595201inversion1nstd223human GRCh38 chr10: 79,542,962-80,217,143 , GRCh37.p13 chr10: 81,302,718-81,976,899 PGGT1BP2, RPS12P18, 29 more genes
    nsv6587639inversion1nstd223human GRCh38 chr10: 79,533,804-80,226,633 , GRCh37.p13 chr10: 81,293,560-81,986,389 SFTPA2, LINC00857, 29 more genes
    nsv6586915inversion1nstd223human GRCh38 chr10: 79,533,787-80,226,538 , GRCh37.p13 chr10: 81,293,543-81,986,294 SFTPA1, ZNRF2P3, 29 more genes
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