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Items: 1 to 20 of 259

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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
    nsv6896408copy number variation1nstd229human GRCh38 chr10: 69,229,781-69,231,610 , GRCh37.p13 chr10: 70,989,537-70,991,366 HKDC1, LOC101928994
    nsv6891721copy number variation1nstd229human GRCh38 chr10: 69,234,052-69,336,830 , GRCh37.p13 chr10: 70,993,808-71,096,586 HK1, RPS15AP28, 1 more genes
    nsv6890865copy number variation1nstd229human GRCh38 chr10: 69,238,368-69,238,678 , GRCh37.p13 chr10: 70,998,124-70,998,434 HKDC1
    nsv6888604copy number variation1nstd229human GRCh38 chr10: 69,264,254-69,277,928 , GRCh37.p13 chr10: 71,024,010-71,037,684 HKDC1, HK1
    nsv6887931copy number variation1nstd229human GRCh38 chr10: 69,232,301-69,362,300 , GRCh37.p13 chr10: 70,992,057-71,122,056 HK1, LOC101928994, 2 more genes
    nsv6886794copy number variation1nstd229human GRCh38 chr10: 69,229,238-69,230,322 , GRCh37.p13 chr10: 70,988,994-70,990,078 HKDC1, LOC101928994
    nsv6884395copy number variation1nstd229human GRCh38 chr10: 69,063,514-69,243,293 , GRCh37.p13 chr10: 70,823,270-71,003,049 SUPV3L1, LOC101928994, 4 more genes
    nsv6883106copy number variation1nstd229human GRCh38 chr10: 69,243,241-69,247,230 , GRCh37.p13 chr10: 71,002,997-71,006,986 HKDC1
    nsv6579433inversion1nstd223human GRCh38 chr10: 69,224,111-69,224,339 , GRCh37.p13 chr10: 70,983,867-70,984,095 LOC101928994, HKDC1
    nsv6444927copy number variation1nstd223human GRCh38 chr10: 69,264,305-69,277,912 , GRCh37.p13 chr10: 71,024,061-71,037,668 HKDC1, HK1
    nsv6438680copy number variation1nstd223human GRCh38 chr10: 69,238,354-69,238,678 , GRCh37.p13 chr10: 70,998,110-70,998,434 HKDC1
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6308916copy number variation1nstd102humanUncertain significance GRCh37 chr10: 67,680,088-71,332,799 , GRCh38.p12 chr10: 65,920,330-69,573,043 RPS3AP38, MIR7151, 62 more genes
    nsv6131969copy number variation1nstd213human GRCh37 chr10: 70,900,000-71,490,001 , GRCh38.p12 chr10: 69,140,244-69,730,245 SUPV3L1, MTND1P20, 19 more genes
    nsv6098392insertion1nstd212human GRCh38 chr10: 69,256,252-69,256,252 , GRCh37.p13 chr10: 71,016,008-71,016,008 HKDC1
    nsv6018197copy number variation1nstd212human GRCh38 chr10: 69,238,362-69,238,684 , GRCh37.p13 chr10: 70,998,118-70,998,440 HKDC1
    nsv5925583copy number variation1nstd209human GRCh38 chr10: 69,238,354-69,238,676 , GRCh37.p13 chr10: 70,998,110-70,998,432 HKDC1
    nsv5925378copy number variation1nstd209human GRCh38 chr10: 69,236,525-69,236,859 , GRCh37.p13 chr10: 70,996,281-70,996,615 HKDC1
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