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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
    nsv6894589copy number variation1nstd229human GRCh38 chr10: 64,506,570-65,063,945 , GRCh37.p13 chr10: 66,266,327-66,823,703 LOC105378335, CYP2C61P, 7 more genes
    nsv6891538copy number variation1nstd229human GRCh38 chr10: 64,216,601-65,524,800 , GRCh37.p13 chr10: 65,976,361-67,284,558 LOC105378336, NEK4P3, 10 more genes
    nsv6881233copy number variation1nstd229human GRCh38 chr10: 64,293,425-66,201,253 , GRCh37.p13 chr10: 66,053,185-67,961,011 CYP2C61P, CTNNA3, 14 more genes
    nsv6878905copy number variation1nstd229human GRCh38 chr10: 63,840,548-66,457,764 , GRCh37.p13 chr10: 65,600,308-68,217,522 LOC105378339, LOC102724863, 19 more genes
    nsv6620652copy number variation1nstd224human GRCh37 chr10: 66,523,544-66,592,466 , GRCh38.p12 chr10: 64,763,787-64,832,709 LOC107984239, LOC105378336, 1 more genes
    nsv6620651copy number variation1nstd224human GRCh37 chr10: 66,492,674-66,592,466 , GRCh38.p12 chr10: 64,732,917-64,832,709 ANXA2P3, CYP2C61P, 2 more genes
    nsv6453765copy number variation1nstd223human GRCh38 chr10: 64,822,825-64,830,105 , GRCh37.p13 chr10: 66,582,582-66,589,862 LOC105378336, ANXA2P3
    nsv6448085copy number variation1nstd223human GRCh38 chr10: 64,797,372-65,548,152 , GRCh37.p13 chr10: 66,557,129-67,307,910 MYL6P3, NEK4P3, 6 more genes
    nsv6447567copy number variation1nstd223human GRCh38 chr10: 64,765,279-64,836,079 , GRCh37.p13 chr10: 66,525,036-66,595,836 LOC107984239, LOC105378336, 1 more genes
    nsv6131962copy number variation1nstd213human GRCh37 chr10: 66,300,000-66,590,001 , GRCh38.p12 chr10: 64,540,243-64,830,244 ANXA2P3, RPL17P35, 4 more genes
    nsv5980442copy number variation1nstd102humanUncertain significance GRCh37 chr10: 66,337,001-67,764,000 , GRCh38.p12 chr10: 64,577,244-66,004,242 NEK4P3, LOC102724863, 13 more genes
    nsv5487125copy number variation1nstd206human GRCh38 chr10: 64,607,896-65,086,270 , GRCh37.p13 chr10: 66,367,653-66,846,028 ANXA2P3, RPL17P35, 7 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976093copy number variation1nstd200human GRCh38 chr10: 64,822,817-64,830,105 , GRCh37.p13 chr10: 66,582,574-66,589,862 LOC105378336, ANXA2P3
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4618056copy number variation1nstd183human GRCh37 chr10: 66,571,457-67,206,761 , GRCh38.p12 chr10: 64,811,700-65,447,003 ANXA2P3, MYL6P3, 5 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
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