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Items: 1 to 20 of 115

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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
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6892495copy number variation1nstd229human GRCh38 chr10: 97,610,807-97,613,602 , GRCh37.p13 chr10: 99,370,564-99,373,359 HOGA1, MORN4
    nsv6889294copy number variation1nstd229human GRCh38 chr10: 97,619,804-97,637,694 , GRCh37.p13 chr10: 99,379,561-99,397,451 MORN4
    nsv6884812copy number variation1nstd229human GRCh38 chr10: 97,607,837-97,615,847 , GRCh37.p13 chr10: 99,367,594-99,375,604 MORN4, HOGA1
    nsv6880683copy number variation1nstd229human GRCh38 chr10: 97,334,301-97,865,700 , GRCh37.p13 chr10: 99,094,058-99,625,457 FRAT2, LOC105378448, 21 more genes
    nsv6880682copy number variation1nstd229human GRCh38 chr10: 97,224,366-98,323,209 , GRCh37.p13 chr10: 98,984,123-100,082,966 ZDHHC16, RPL34P20, 29 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6588928inversion1nstd223human GRCh38 chr10: 97,628,670-97,629,155 , GRCh37.p13 chr10: 99,388,427-99,388,912 MORN4
    nsv6580724inversion1nstd223human GRCh38 chr10: 97,613,094-97,613,571 , GRCh37.p13 chr10: 99,372,851-99,373,328 HOGA1, MORN4
    nsv6438100copy number variation1nstd223human GRCh38 chr10: 97,619,804-97,637,690 , GRCh37.p13 chr10: 99,379,561-99,397,447 MORN4
    nsv6314071copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,070,594-99,445,724 , GRCh38.p12 chr10: 97,310,837-97,685,967 AVPI1, ANKRD2, 15 more genes
    nsv6018270copy number variation1nstd212human GRCh38 chr10: 97,608,782-97,619,302 , GRCh37.p13 chr10: 99,368,539-99,379,059 HOGA1, MORN4
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv4986865copy number variation1nstd200human GRCh38 chr10: 97,619,804-97,637,690 , GRCh37.p13 chr10: 99,379,561-99,397,447 MORN4
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4187228copy number variation1nstd166human GRCh37.p13 chr10: 99,355,000-99,398,000 , GRCh38.p12 chr10: 97,595,243-97,638,243 HOGA1, MORN4
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