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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683629copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 17,345,376-17,380,514 , GRCh38.p12 chr1: 17,018,881-17,054,019 SDHB
    nsv6310921copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,349,093-17,380,514 , GRCh38.p12 chr1: 17,022,598-17,054,019 SDHB
    nsv5673240copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,376-17,371,403 , GRCh38.p12 chr1: 17,018,881-17,044,908 SDHB
    nsv4682910copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,366-17,371,393 , GRCh38.p12 chr1: 17,018,871-17,044,898 SDHB
    nsv3873900copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,018,875-17,044,894 , GRCh37 chr1: 17,345,370-17,371,389 SDHB
    nsv4683305copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 17,345,376-17,371,393 , GRCh38.p12 chr1: 17,018,881-17,044,898 SDHB
    nsv7095713copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,359,545-17,380,514 , GRCh38.p12 chr1: 17,033,050-17,054,019 SDHB
    nsv3882531copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,048,754-17,064,432 , GRCh37 chr1: 17,375,249-17,390,927 SDHB
    nsv6314872copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,048,756-17,064,430 , GRCh37.p13 chr1: 17,375,251-17,390,925 SDHB
    nsv4683776copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,366-17,359,650 , GRCh38.p12 chr1: 17,018,871-17,033,155 SDHB
    nsv3873146copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,370-17,359,646 , GRCh38 chr1: 17,018,875-17,033,151 SDHB
    nsv6310920copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,376-17,359,650 , GRCh38.p12 chr1: 17,018,881-17,033,155 SDHB
    nsv4681738copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,371,246-17,380,514 , GRCh38.p12 chr1: 17,044,751-17,054,019 SDHB
    nsv5059995copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,029,670-17,037,574 , GRCh37 chr1: 17,356,165-17,364,069 SDHB
    nsv4452797copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,044,751-17,044,898 , GRCh37 chr1: 17,371,246-17,371,393 SDHB
    nsv3871759copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,044,761-17,044,888 , GRCh37 chr1: 17,371,256-17,371,383 SDHB
    nsv3883449copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,033,050-17,033,155 , GRCh37 chr1: 17,359,545-17,359,650 SDHB
    nsv4452282copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,018,871-17,018,968 , GRCh37 chr1: 17,345,366-17,345,463 SDHB
    nsv3884164copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,359,549-17,359,646 , GRCh38 chr1: 17,033,054-17,033,151 SDHB
    nsv3887326copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,053,938-17,054,029 , GRCh37 chr1: 17,380,433-17,380,524 SDHB
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