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Items: 1 to 20 of 193

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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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093857copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,648,810-105,677,352 , GRCh38.p12 chr10: 103,889,052-103,917,594 STN1
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6894946copy number variation1nstd229human GRCh38 chr10: 103,888,277-103,888,454 , GRCh37.p13 chr10: 105,648,035-105,648,212 STN1
    nsv6889111copy number variation1nstd229human GRCh38 chr10: 103,916,239-103,922,327 , GRCh37.p13 chr10: 105,675,997-105,682,085 STN1
    nsv6881113copy number variation1nstd229human GRCh38 chr10: 103,887,263-103,918,225 , GRCh37.p13 chr10: 105,647,021-105,677,983 STN1
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6637523copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,015,345-105,911,204 , GRCh38.p12 chr10: 103,255,588-104,151,446 PCGF6, INA, 20 more genes
    nsv6620153copy number variation1nstd224human GRCh37 chr10: 105,647,095-105,677,897 , GRCh38.p12 chr10: 103,887,337-103,918,139 STN1
    nsv6314221insertion1nstd102humanUncertain significance GRCh38 chr10: 103,900,166-103,900,166 , GRCh37 chr10: 105,659,924-105,659,924 STN1
    nsv6308899copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,642,442-105,677,352 , GRCh38.p12 chr10: 103,882,684-103,917,594 STN1
    nsv6283955insertion1nstd214human GRCh38 chr10: 103,909,436-103,909,436 , GRCh37.p13 chr10: 105,669,194-105,669,194 STN1
    nsv6281622insertion1nstd214human GRCh38 chr10: 103,909,376-103,909,376 , GRCh37.p13 chr10: 105,669,134-105,669,134 STN1
    nsv6281501insertion1nstd214human GRCh38 chr10: 103,909,500-103,909,500 , GRCh37.p13 chr10: 105,669,258-105,669,258 STN1
    nsv6279367insertion1nstd214human GRCh38 chr10: 103,909,490-103,909,490 , GRCh37.p13 chr10: 105,669,248-105,669,248 STN1
    nsv6279069insertion1nstd214human GRCh38 chr10: 103,909,372-103,909,372 , GRCh37.p13 chr10: 105,669,130-105,669,130 STN1
    nsv6278411insertion1nstd214human GRCh38 chr10: 103,909,520-103,909,520 , GRCh37.p13 chr10: 105,669,278-105,669,278 STN1
    nsv6186757copy number variation1nstd214human GRCh38 chr10: 103,909,372-103,909,423 , GRCh37.p13 chr10: 105,669,130-105,669,181 STN1
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