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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7069508inversion1nstd229human GRCh38 chr15: 51,686,723-51,694,467 , GRCh37.p13 chr15: 51,978,920-51,986,664 SCG3
    nsv7059635inversion1nstd229human GRCh38 chr15: 51,716,761-55,548,818 , GRCh37.p13 chr15: 52,008,958-55,841,016 CCPG1, LOC105370823, 51 more genes
    nsv6973840copy number variation1nstd229human GRCh38 chr15: 51,686,413-51,687,403 , GRCh37.p13 chr15: 51,978,610-51,979,600 SCG3
    nsv6967849copy number variation1nstd229human GRCh38 chr15: 51,719,180-51,719,226 , GRCh37.p13 chr15: 52,011,377-52,011,423 SCG3
    nsv6967577copy number variation1nstd229human GRCh38 chr15: 51,697,834-51,698,025 , GRCh37.p13 chr15: 51,990,031-51,990,222 SCG3
    nsv6966440copy number variation1nstd229human GRCh38 chr15: 51,691,911-51,691,965 , GRCh37.p13 chr15: 51,984,108-51,984,162 SCG3
    nsv6958703copy number variation1nstd229human GRCh38 chr15: 51,697,177-51,697,290 , GRCh37.p13 chr15: 51,989,374-51,989,487 SCG3
    nsv6638084insertion1nstd102humanUncertain significance GRCh38 chr15: 51,686,717-51,686,717 , GRCh37 chr15: 51,978,914-51,978,914 SCG3
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6591237inversion1nstd223human GRCh38 chr15: 51,686,722-51,694,467 , GRCh37.p13 chr15: 51,978,919-51,986,664 SCG3
    nsv6584915inversion1nstd223human GRCh38 chr15: 51,708,614-51,709,884 , GRCh37.p13 chr15: 52,000,811-52,002,081 SCG3
    nsv6500722copy number variation1nstd223human GRCh38 chr15: 51,721,031-51,730,778 , GRCh37.p13 chr15: 52,013,228-52,022,975 SCG3, LYSMD2
    nsv6495675copy number variation1nstd223human GRCh38 chr15: 51,697,177-51,697,290 , GRCh37.p13 chr15: 51,989,374-51,989,487 SCG3
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6290450copy number variation1nstd102humanUncertain significance GRCh38 chr15: 51,681,311-51,791,472 , GRCh37.p13 chr15: 51,973,508-52,083,669 TMOD2, SCG3, 1 more genes
    nsv6242066mobile element insertion1nstd215human GRCh38 chr15: 51,698,809-51,698,809 , GRCh37.p13 chr15: 51,991,006-51,991,006 SCG3
    nsv6197398copy number variation1nstd214human GRCh38 chr15: 51,691,911-51,691,964 , GRCh37.p13 chr15: 51,984,108-51,984,161 SCG3
    nsv6132897copy number variation1nstd213human GRCh37 chr15: 50,000,000-53,730,001 , GRCh38.p12 chr15: 49,707,803-53,437,804 MAPK6, ARPP19, 65 more genes
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