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Items: 1 to 20 of 116

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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
    nsv7061919inversion1nstd229human GRCh38 chr10: 114,017,010-114,074,417 , GRCh37.p13 chr10: 115,776,769-115,834,176 LOC105378493, ADRB1, 1 more genes
    nsv6893042copy number variation1nstd229human GRCh38 chr10: 114,019,014-114,029,257 , GRCh37.p13 chr10: 115,778,773-115,789,016 LOC105378492, LOC105378493
    nsv6892037copy number variation1nstd229human GRCh38 chr10: 114,017,233-114,033,403 , GRCh37.p13 chr10: 115,776,992-115,793,162 LOC105378492, LOC105378493
    nsv6887065copy number variation1nstd229human GRCh38 chr10: 114,022,607-114,023,410 , GRCh37.p13 chr10: 115,782,366-115,783,169 LOC105378492
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6132019copy number variation1nstd213human GRCh37 chr10: 115,120,000-116,220,001 , GRCh38.p12 chr10: 113,360,241-114,460,242 CASP7, MIR2110, 21 more genes
    nsv6131849copy number variation1nstd213human GRCh37 chr10: 115,460,000-116,120,001 , GRCh38.p12 chr10: 113,700,241-114,360,242 ADRB1, CASP7, 15 more genes
    nsv5373292translocation1nstd200human GRCh38 chr10: 114,025,147-114,025,147 , GRCh38 chr10: 114,015,250-114,015,250 , GRCh37.p13 chr10: 115,775,009-115,775,009 , GRCh37.p13 chr10: 115,784,906-115,784,906 LOC105378492
    nsv5373291translocation1nstd200human GRCh38 chr10: 114,024,838-114,024,838 , GRCh38 chr10: 114,015,229-114,015,229 , GRCh37.p13 chr10: 115,774,988-115,774,988 , GRCh37.p13 chr10: 115,784,597-115,784,597 LOC105378492
    nsv5341377translocation1nstd200human GRCh37 chr10: 115,784,597-115,784,597 , GRCh37 chr10: 115,774,988-115,774,988 , GRCh38.p12 chr10: 114,015,229-114,015,229 , GRCh38.p12 chr10: 114,024,838-114,024,838 LOC105378492
    nsv5340871translocation1nstd200human GRCh37 chr10: 115,775,009-115,775,009 , GRCh37 chr10: 115,784,906-115,784,906 , GRCh38.p12 chr10: 114,025,147-114,025,147 , GRCh38.p12 chr10: 114,015,250-114,015,250 LOC105378492
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5133996mobile element insertion1nstd203human GRCh38 chr10: 114,012,220-114,012,258 , GRCh37.p13 chr10: 115,771,979-115,772,017 LOC105378492
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4880587inversion1nstd200human GRCh37 chr10: 115,288,028-117,482,906 , GRCh38.p12 chr10: 113,528,269-115,723,396 , NHLRC2, 31 more genes
    nsv4603726copy number variation1nstd183human GRCh37 chr10: 115,775,099-115,792,731 , GRCh38.p12 chr10: 114,015,340-114,032,972 LOC105378492, LOC105378493
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