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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099220copy number variation1nstd231human GRCh38.p12 chr1: 101,582,985-103,037,160 , GRCh37 chr1: 102,048,541-103,502,716 COL11A1, DNAJA1P5, 9 more genes
    nsv7055743inversion1nstd229human GRCh38 chr1: 102,094,047-102,098,295 , GRCh37.p13 chr1: 102,559,603-102,563,851 LOC107985095
    nsv7047240inversion1nstd229human GRCh38 chr1: 101,939,267-103,207,438 , GRCh37.p13 chr1: 102,404,823-103,672,994 SOD2P1, LOC107985096, 5 more genes
    nsv7046675inversion1nstd229human GRCh38 chr1: 101,693,247-102,832,942 , GRCh37.p13 chr1: 102,158,803-103,298,498 OLFM3, RNU6-352P, 8 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
    nsv6638302copy number variation1nstd229human GRCh38 chr1: 101,670,769-103,274,061 , GRCh37.p13 chr1: 102,136,325-103,739,617 RNU6-965P, LOC112268286, 10 more genes
    nsv6638217copy number variation1nstd229human GRCh38 chr1: 102,092,977-102,103,509 , GRCh37.p13 chr1: 102,558,533-102,569,065 LOC107985095
    nsv6638216copy number variation1nstd229human GRCh38 chr1: 102,087,760-102,099,728 , GRCh37.p13 chr1: 102,553,316-102,565,284 LOC107985095
    nsv6638215copy number variation1nstd229human GRCh38 chr1: 102,087,723-102,091,924 , GRCh37.p13 chr1: 102,553,279-102,557,480 LOC107985095
    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
    nsv6636361copy number variation1nstd102humanUncertain significance GRCh37 chr1: 102,401,870-103,784,459 , GRCh38.p12 chr1: 101,936,314-103,318,901 SOD2P1, COL11A1, 5 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
    nsv6290372copy number variation1nstd102humanUncertain significance GRCh37 chr1: 101,991,785-103,555,759 , GRCh38.p12 chr1: 101,526,229-103,090,203 RNU6-965P, LOC112268286, 9 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
    nsv6133542copy number variation1nstd213human GRCh37 chr1: 101,420,000-103,740,001 , GRCh38.p12 chr1: 100,954,444-103,274,445 PPIAP7, SLC30A7, 20 more genes
    nsv6056126insertion1nstd212human GRCh38 chr1: 102,093,615-102,093,615 , GRCh37.p13 chr1: 102,559,171-102,559,171 LOC107985095
    nsv6055985insertion1nstd212human GRCh38 chr1: 102,093,582-102,093,582 , GRCh37.p13 chr1: 102,559,138-102,559,138 LOC107985095
    nsv6052904insertion1nstd212human GRCh38 chr1: 102,093,648-102,093,648 , GRCh37.p13 chr1: 102,559,204-102,559,204 LOC107985095
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