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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 more genes
    nsv7046848inversion1nstd229human GRCh38 chr1: 160,681,442-160,681,504 , GRCh37.p13 chr1: 160,651,232-160,651,294 CD48
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643352copy number variation1nstd229human GRCh38 chr1: 160,655,832-160,802,833 , GRCh37.p13 chr1: 160,625,622-160,772,623 CD48, SETP9, 3 more genes
    nsv6643252copy number variation1nstd229human GRCh38 chr1: 160,678,567-160,678,763 , GRCh37.p13 chr1: 160,648,357-160,648,553 CD48
    nsv6643135copy number variation1nstd229human GRCh38 chr1: 160,693,211-160,702,348 , GRCh37.p13 chr1: 160,663,001-160,672,138 CD48
    nsv6637035copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,778,364-160,770,515 , GRCh38.p12 chr1: 159,808,574-160,800,725 PEX19, SLAMF8, 43 more genes
    nsv6552401inversion1nstd223human GRCh38 chr1: 160,704,355-160,705,437 , GRCh37.p13 chr1: 160,674,145-160,675,227 CD48
    nsv6333545copy number variation1nstd223human GRCh38 chr1: 160,690,902-160,699,271 , GRCh37.p13 chr1: 160,660,692-160,669,061 CD48
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6331023copy number variation1nstd223human GRCh38 chr1: 160,682,661-160,683,589 , GRCh37.p13 chr1: 160,652,451-160,653,379 CD48
    nsv6325678copy number variation1nstd223human GRCh38 chr1: 160,699,101-160,700,000 , GRCh37.p13 chr1: 160,668,891-160,669,790 CD48
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 USF1, TRE-CTC1-3, 161 more genes
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6308884mobile element deletion1nstd186human GRCh37 chr1: 160,660,738-160,669,008 , GRCh38.p12 chr1: 160,690,948-160,699,218 CD48
    nsv6245318mobile element insertion1nstd215human GRCh38 chr1: 160,706,718-160,706,718 , GRCh37.p13 chr1: 160,676,508-160,676,508 CD48
    nsv6147402mobile element deletion1nstd206human GRCh38 chr1: 160,690,948-160,699,218 , GRCh37.p13 chr1: 160,660,738-160,669,008 CD48
    nsv6147217mobile element deletion1nstd206human GRCh38 chr1: 160,691,932-160,699,958 , GRCh37.p13 chr1: 160,661,722-160,669,748 CD48
    nsv6138749copy number variation1nstd206human GRCh38 chr1: 160,690,587-160,700,587 , GRCh37.p13 chr1: 160,660,377-160,670,377 CD48
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