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Items: 1 to 20 of 372

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099181copy number variation1nstd231human GRCh38.p12 chr1: 18,899,486-20,046,918 , GRCh37 chr1: 19,225,980-20,373,411 CAPZB, HTR6, 32 more genes
    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
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 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
    nsv7048467inversion1nstd229human GRCh38 chr1: 19,692,048-19,698,199 , GRCh37.p13 chr1: 20,018,541-20,024,692 TMCO4
    nsv7041312inversion1nstd229human GRCh38 chr1: 19,776,598-19,776,837 , GRCh37.p13 chr1: 20,103,091-20,103,330 TMCO4
    nsv6646964copy number variation1nstd229human GRCh38 chr1: 19,796,913-19,809,722 , GRCh37.p13 chr1: 20,123,406-20,136,215 TMCO4
    nsv6646963copy number variation1nstd229human GRCh38 chr1: 19,756,418-19,762,623 , GRCh37.p13 chr1: 20,082,911-20,089,116 TMCO4
    nsv6646962copy number variation1nstd229human GRCh38 chr1: 19,727,243-19,735,760 , GRCh37.p13 chr1: 20,053,736-20,062,253 TMCO4
    nsv6646901copy number variation1nstd229human GRCh38 chr1: 19,781,001-19,812,500 , GRCh37.p13 chr1: 20,107,494-20,138,993 RNF186, TMCO4
    nsv6646900copy number variation1nstd229human GRCh38 chr1: 19,768,696-19,772,118 , GRCh37.p13 chr1: 20,095,189-20,098,611 TMCO4
    nsv6646899copy number variation1nstd229human GRCh38 chr1: 19,751,232-20,412,088 , GRCh37.p13 chr1: 20,077,725-20,738,581 LOC105376826, LOC105376823, 17 more genes
    nsv6646898copy number variation1nstd229human GRCh38 chr1: 19,723,241-19,744,671 , GRCh37.p13 chr1: 20,049,734-20,071,164 TMCO4
    nsv6646897copy number variation1nstd229human GRCh38 chr1: 19,720,870-19,729,134 , GRCh37.p13 chr1: 20,047,363-20,055,627 TMCO4
    nsv6646896copy number variation1nstd229human GRCh38 chr1: 19,702,029-19,707,181 , GRCh37.p13 chr1: 20,028,522-20,033,674 TMCO4
    nsv6646811copy number variation1nstd229human GRCh38 chr1: 19,714,746-19,720,382 , GRCh37.p13 chr1: 20,041,239-20,046,875 TMCO4
    nsv6646810copy number variation1nstd229human GRCh38 chr1: 19,700,001-19,704,800 , GRCh37.p13 chr1: 20,026,494-20,031,293 TMCO4
    nsv6646809copy number variation1nstd229human GRCh38 chr1: 19,694,007-19,698,796 , GRCh37.p13 chr1: 20,020,500-20,025,289 TMCO4
    nsv6646808copy number variation1nstd229human GRCh38 chr1: 19,688,032-19,703,404 , GRCh37.p13 chr1: 20,014,525-20,029,897 TMCO4
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