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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7093903copy number variation1nstd102humanUncertain significance GRCh37 chr10: 95,891,911-96,087,866 , GRCh38.p12 chr10: 94,132,154-94,328,109 RNU6-657P, NOC3L, 3 more genes
    nsv6898002copy number variation1nstd229human GRCh38 chr10: 94,353,819-94,382,685 , GRCh37.p13 chr10: 96,113,576-96,142,442 NOC3L
    nsv6897956copy number variation1nstd229human GRCh38 chr10: 94,347,501-94,351,200 , GRCh37.p13 chr10: 96,107,258-96,110,957 NOC3L
    nsv6892443copy number variation1nstd229human GRCh38 chr10: 94,327,321-94,332,211 , GRCh37.p13 chr10: 96,087,078-96,091,968 PLCE1, NOC3L
    nsv6890548copy number variation1nstd229human GRCh38 chr10: 93,867,543-94,344,766 , GRCh37.p13 chr10: 95,627,300-96,104,523 HDAC1P1, LOC107984255, 10 more genes
    nsv6880933copy number variation1nstd229human GRCh38 chr10: 94,289,901-94,343,500 , GRCh37.p13 chr10: 96,049,658-96,103,257 NOC3L, PLCE1
    nsv6595352inversion1nstd223human GRCh38 chr10: 94,336,329-94,336,972 , GRCh37.p13 chr10: 96,096,086-96,096,729 NOC3L
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6582387inversion1nstd223human GRCh38 chr10: 94,349,756-94,350,715 , GRCh37.p13 chr10: 96,109,513-96,110,472 NOC3L
    nsv6453406copy number variation1nstd223human GRCh38 chr10: 94,346,970-94,347,420 , GRCh37.p13 chr10: 96,106,727-96,107,177 NOC3L
    nsv6441330copy number variation1nstd223human GRCh38 chr10: 94,347,701-94,348,800 , GRCh37.p13 chr10: 96,107,458-96,108,557 NOC3L
    nsv6294549mobile element insertion1nstd186human GRCh37 chr10: 96,094,565-96,094,616 , GRCh38.p12 chr10: 94,334,808-94,334,859 NOC3L
    nsv6247388mobile element insertion1nstd215human GRCh38 chr10: 94,329,444-94,329,444 , GRCh37.p13 chr10: 96,089,201-96,089,201 PLCE1, NOC3L
    nsv6132060copy number variation1nstd213human GRCh37 chr10: 95,430,000-96,160,001 , GRCh38.p12 chr10: 93,670,243-94,400,244 LGI1, PLCE1, 14 more genes
    nsv6131987copy number variation1nstd213human GRCh37 chr10: 96,000,000-98,330,001 , GRCh38.p12 chr10: 94,240,243-96,570,244 ENTPD1, CYP2C19, 39 more genes
    nsv6131986copy number variation1nstd213human GRCh37 chr10: 95,390,000-96,170,001 , GRCh38.p12 chr10: 93,630,243-94,410,244 PDE6C, LGI1, 16 more genes
    nsv6131898copy number variation1nstd213human GRCh37 chr10: 95,390,000-96,200,001 , GRCh38.p12 chr10: 93,630,243-94,440,244 PDE6C, LGI1, 16 more genes
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