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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv6995647copy number variation1nstd229human GRCh38 chr16: 67,457,801-67,460,300 , GRCh37.p13 chr16: 67,491,704-67,494,203 ATP6V0D1
    nsv6993028copy number variation1nstd229human GRCh38 chr16: 67,439,353-67,443,097 , GRCh37.p13 chr16: 67,473,256-67,477,000 ATP6V0D1
    nsv6992862copy number variation1nstd229human GRCh38 chr16: 67,372,949-67,543,806 , GRCh37.p13 chr16: 67,406,852-67,577,709 AGRP, RNU1-123P, 8 more genes
    nsv6983006copy number variation1nstd229human GRCh38 chr16: 67,480,484-67,496,712 , GRCh37.p13 chr16: 67,514,387-67,530,615 ATP6V0D1-DT, AGRP, 1 more genes
    nsv6980876copy number variation1nstd229human GRCh38 chr16: 67,479,917-67,480,220 , GRCh37.p13 chr16: 67,513,820-67,514,123 ATP6V0D1-DT, ATP6V0D1
    nsv6503035copy number variation1nstd223human GRCh38 chr16: 67,480,530-67,496,729 , GRCh37.p13 chr16: 67,514,433-67,530,632 AGRP, ATP6V0D1-DT, 1 more genes
    nsv6496728copy number variation1nstd223human GRCh38 chr16: 67,479,778-67,480,198 , GRCh37.p13 chr16: 67,513,681-67,514,101 ATP6V0D1, ATP6V0D1-DT
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6132997copy number variation1nstd213human GRCh37 chr16: 67,360,000-67,510,001 , GRCh38.p12 chr16: 67,326,097-67,476,098 HSD11B2, ATP6V0D1, 5 more genes
    nsv6121309copy number variation1nstd186human GRCh37 chr16: 67,513,820-67,514,123 , GRCh38.p12 chr16: 67,479,917-67,480,220 ATP6V0D1-DT, ATP6V0D1
    nsv6099458insertion1nstd212human GRCh38 chr16: 67,472,962-67,472,962 , GRCh37.p13 chr16: 67,506,865-67,506,865 ATP6V0D1
    nsv6025499copy number variation1nstd212human GRCh38 chr16: 67,479,904-67,480,221 , GRCh37.p13 chr16: 67,513,807-67,514,124 ATP6V0D1-DT, ATP6V0D1
    nsv5943349copy number variation1nstd209human GRCh38 chr16: 67,447,622-67,447,713 , GRCh37.p13 chr16: 67,481,525-67,481,616 ATP6V0D1
    nsv5940830copy number variation1nstd209human GRCh38 chr16: 67,471,402-67,472,842 , GRCh37.p13 chr16: 67,505,305-67,506,745 ATP6V0D1
    nsv5937054copy number variation1nstd209human GRCh38 chr16: 67,479,902-67,480,219 , GRCh37.p13 chr16: 67,513,805-67,514,122 ATP6V0D1-DT, ATP6V0D1
    nsv5878413copy number variation1nstd209human GRCh38 chr16: 67,471,369-67,473,015 , GRCh37.p13 chr16: 67,505,272-67,506,918 ATP6V0D1
    nsv5593672copy number variation1nstd207human GRCh38 chr16: 67,479,902-67,480,219 , GRCh37.p13 chr16: 67,513,805-67,514,122 ATP6V0D1-DT, ATP6V0D1
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