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Items: 1 to 20 of 1097

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099221copy number variation1nstd231human GRCh38.p12 chr1: 103,068,865-105,809,051 , GRCh37 chr1: 103,534,421-106,351,673 AMY1A, AMY1B, 21 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6638470copy number variation1nstd229human GRCh38 chr1: 102,981,109-105,059,265 , GRCh37.p13 chr1: 103,446,665-105,601,887 RNPC3, LOC105378878, 16 more genes
    nsv6638119copy number variation1nstd229human GRCh38 chr1: 101,264,431-104,423,425 , GRCh37.p13 chr1: 101,729,987-104,966,047 RNU6-352P, PPIAP7, 28 more genes
    nsv6635768copy number variation1nstd227human GRCh38.p12 chr1: 103,551,915-103,902,694 , GRCh37 chr1: 104,094,537-104,445,316 AMY1A, AMY1B, 7 more genes
    nsv6625473copy number variation11nstd224human GRCh37 chr1: 104,113,158-104,297,239 , GRCh38.p12 chr1: 103,570,536-103,754,617 AMY1A, AMY1B, 6 more genes
    nsv6625336copy number variation1nstd224human GRCh37 chr1: 104,113,158-104,315,458 , GRCh38.p12 chr1: 103,570,536-103,772,836 AMY1A, AMY1B, 6 more genes
    nsv6625073copy number variation2nstd224human GRCh37 chr1: 104,093,571-104,297,239 , GRCh38.p12 chr1: 103,550,949-103,754,617 AMY1A, AMY1B, 7 more genes
    nsv6547529inversion1nstd223human GRCh38 chr1: 101,361,683-104,587,052 , GRCh37.p13 chr1: 101,827,239-105,129,674 AMY1C, AMYP1, 26 more genes
    nsv6323500copy number variation1nstd223human GRCh38 chr1: 101,264,431-104,423,425 , GRCh37.p13 chr1: 101,729,987-104,966,047 RPSAP19, LOC105378874, 28 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6296911copy number variation1nstd186human GRCh37 chr1: 104,136,622-104,302,822 , GRCh38.p12 chr1: 103,594,000-103,760,200 AMY1A, AMY1B, 4 more genes
    nsv6290366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608 LOC105379827, RPSAP19, 63 more genes
    nsv6290066copy number variation1nstd218human GRCh37 chr1: 104,107,530-104,307,708 , GRCh38.p12 chr1: 103,564,908-103,765,086 AMY1A, AMY1B, 6 more genes
    nsv6138520copy number variation1nstd206human GRCh38 chr1: 103,593,835-103,957,835 , GRCh37.p13 chr1: 104,136,457-104,500,457 AMY1A, AMY1B, 5 more genes
    nsv6138078copy number variation1nstd206human GRCh38 chr1: 103,594,000-103,760,200 , GRCh37.p13 chr1: 104,136,622-104,302,822 AMY1A, AMY1B, 4 more genes
    nsv6133543copy number variation1nstd213human GRCh37 chr1: 103,920,000-104,550,001 , GRCh38.p12 chr1: 103,377,378-104,007,379 AMY1A, AMY1B, 10 more genes
    nsv6102180inversion1nstd212human GRCh38 chr1: 103,618,774-103,667,876 , GRCh37.p13 chr1: 104,161,396-104,210,498 AMY1A, AMY2A
    nsv5980625copy number variation1nstd212human GRCh38 chr1: 103,561,098-103,676,921 , GRCh37.p13 chr1: 104,103,720-104,219,543 AMY1A, AMY2A, 2 more genes
    nsv5432744copy number variation1nstd206human GRCh38 chr1: 103,593,835-103,760,800 , GRCh37.p13 chr1: 104,136,457-104,303,422 AMY1A, AMY1B, 4 more genes
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