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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5979500inversion1nstd209human GRCh38 chr21: 22,252,993-27,920,987 , GRCh37.p13 chr21: 23,625,313-29,293,306 , APP, 60 more genes
    nsv5975652insertion1nstd209human GRCh38 chr21: 23,370,205-23,370,205 , GRCh37.p13 chr21: 24,742,527-24,742,527 D21S2088E
    nsv5964034copy number variation1nstd209human GRCh38 chr21: 23,384,483-23,389,152 , GRCh37.p13 chr21: 24,756,804-24,761,473 D21S2088E, EEF1A1P1
    nsv5962007copy number variation1nstd209human GRCh38 chr21: 23,369,182-23,370,823 , GRCh37.p13 chr21: 24,741,504-24,743,145 D21S2088E
    nsv5954844copy number variation1nstd209human GRCh38 chr21: 23,369,910-23,370,223 , GRCh37.p13 chr21: 24,742,232-24,742,545 D21S2088E
    nsv5952474copy number variation1nstd209human GRCh38 chr21: 23,367,571-23,368,866 , GRCh37.p13 chr21: 24,739,893-24,741,188 D21S2088E
    nsv5950424copy number variation1nstd209human GRCh38 chr21: 23,354,500-23,359,663 , GRCh37.p13 chr21: 24,726,822-24,731,985 D21S2088E
    nsv5869210copy number variation1nstd209human GRCh38 chr21: 23,384,172-23,388,821 , GRCh37.p13 chr21: 24,756,493-24,761,142 EEF1A1P1, D21S2088E
    nsv5591605copy number variation1nstd207human GRCh38 chr21: 23,369,910-23,370,223 , GRCh37.p13 chr21: 24,742,232-24,742,545 D21S2088E
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5525423copy number variation1nstd206human GRCh38 chr21: 23,369,924-23,370,224 , GRCh37.p13 chr21: 24,742,246-24,742,546 D21S2088E
    nsv5523764copy number variation1nstd206human GRCh38 chr21: 23,352,174-23,360,351 , GRCh37.p13 chr21: 24,724,496-24,732,673 D21S2088E
    nsv5521378copy number variation1nstd206human GRCh38 chr21: 23,384,483-23,389,153 , GRCh37.p13 chr21: 24,756,804-24,761,474 EEF1A1P1, D21S2088E
    nsv5515164copy number variation1nstd206human GRCh38 chr21: 23,365,507-23,424,877 , GRCh37.p13 chr21: 24,737,829-24,797,197 TUBAP1, EEF1A1P1, 3 more genes
    nsv5382231mobile element deletion2nstd186human GRCh37 chr21: 24,742,246-24,742,546 , GRCh38.p12 chr21: 23,369,924-23,370,224 D21S2088E
    nsv5216888mobile element deletion1nstd204human GRCh38.p13 chr21: 23,369,857-23,370,253 , GRCh37.p13 chr21: 24,742,179-24,742,575 D21S2088E
    nsv5171382mobile element insertion1nstd203human GRCh38 chr21: 23,370,205-23,370,231 , GRCh37.p13 chr21: 24,742,527-24,742,553 D21S2088E
    nsv5170152mobile element insertion1nstd203human GRCh38 chr21: 23,370,168-23,370,205 , GRCh37.p13 chr21: 24,742,490-24,742,527 D21S2088E
    nsv5036990inversion1nstd200human GRCh38 chr21: 21,590,024-25,090,354 , GRCh37.p13 chr21: 22,962,345-26,462,667 , LINC01692, 25 more genes
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