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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6646844copy number variation1nstd229human GRCh38 chr1: 18,851,610-18,862,753 , GRCh37.p13 chr1: 19,178,104-19,189,247 TAS1R2
    nsv6646761copy number variation1nstd229human GRCh38 chr1: 18,857,353-18,863,592 , GRCh37.p13 chr1: 19,183,847-19,190,086 TAS1R2
    nsv6646679copy number variation1nstd229human GRCh38 chr1: 18,854,016-18,914,889 , GRCh37.p13 chr1: 19,180,510-19,241,383 TAS1R2, ALDH4A1, 3 more genes
    nsv6646673copy number variation1nstd229human GRCh38 chr1: 18,837,456-18,870,489 , GRCh37.p13 chr1: 19,163,950-19,196,983 TAS1R2, ALDH4A1
    nsv6646589copy number variation1nstd229human GRCh38 chr1: 18,782,901-19,372,400 , GRCh37.p13 chr1: 19,109,395-19,698,894 MIR4695, AKR7A3, 15 more genes
    nsv6646349copy number variation1nstd229human GRCh38 chr1: 18,567,401-18,926,100 , GRCh37.p13 chr1: 18,893,895-19,252,594 ALDH4A1, PAX7, 4 more genes
    nsv6646163copy number variation1nstd229human GRCh38 chr1: 18,448,924-18,911,123 , GRCh37.p13 chr1: 18,775,418-19,237,617 KLHDC7A, MIR1290, 6 more genes
    nsv6646155copy number variation1nstd229human GRCh38 chr1: 18,854,881-18,855,968 , GRCh37.p13 chr1: 19,181,375-19,182,462 TAS1R2
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6290472copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580 MIR1290, RNU6-1099P, 92 more genes
    nsv6214481insertion1nstd214human GRCh38 chr1: 18,858,186-18,858,186 , GRCh37.p13 chr1: 19,184,680-19,184,680 TAS1R2
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
    nsv6133609copy number variation1nstd213human GRCh37 chr1: 18,830,000-19,700,001 , GRCh38.p12 chr1: 18,503,506-19,373,507 CAPZB, PAX7, 17 more genes
    nsv6133572copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,950,001 , GRCh38.p12 chr1: 16,943,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5872990copy number variation1nstd209human GRCh38 chr1: 18,854,881-18,855,967 , GRCh37.p13 chr1: 19,181,375-19,182,461 TAS1R2
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