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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147187copy number variation1nstd232human GRCh37.p13 chr17: 61,899,002-61,899,080 , GRCh38.p12 chr17: 63,821,642-63,821,720 FTSJ3
    nsv7145537copy number variation1nstd232human GRCh37.p13 chr17: 61,897,354-61,897,437 , GRCh38.p12 chr17: 63,819,994-63,820,077 FTSJ3
    nsv7140934copy number variation1nstd232human GRCh37.p13 chr17: 61,902,097-61,902,183 , GRCh38.p12 chr17: 63,824,737-63,824,823 FTSJ3
    nsv7140003copy number variation1nstd232human GRCh37.p13 chr17: 61,898,298-61,898,388 , GRCh38.p12 chr17: 63,820,938-63,821,028 FTSJ3
    nsv7138509copy number variation1nstd232human GRCh37.p13 chr17: 61,897,533-61,897,613 , GRCh38.p12 chr17: 63,820,173-63,820,253 FTSJ3
    nsv7138300copy number variation1nstd232human GRCh37.p13 chr17: 61,901,599-61,901,689 , GRCh38.p12 chr17: 63,824,239-63,824,329 FTSJ3
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv6990462copy number variation1nstd229human GRCh38 chr17: 63,821,394-63,821,493 , GRCh37.p13 chr17: 61,898,754-61,898,853 FTSJ3
    nsv6637179copy number variation1nstd102humanUncertain significance GRCh37 chr17: 61,838,634-62,465,444 , GRCh38.p12 chr17: 63,761,274-64,469,327 GH2, DDX42, 24 more genes
    nsv6250948mobile element insertion1nstd215human GRCh37.p13 chr17: 61,903,600-61,903,600 , GRCh38 chr17: 63,826,240-63,826,240 , PSMC5, 1 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5699043mobile element insertion1nstd211human GRCh38 chr17: 63,826,240-63,826,240 , GRCh37.p13 chr17: 61,903,600-61,903,600 , PSMC5, 1 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531754copy number variation1nstd206human GRCh38 chr17: 63,821,424-63,821,502 , GRCh37.p13 chr17: 61,898,784-61,898,862 FTSJ3
    nsv5424992mobile element insertion1nstd206human GRCh38 chr17: 63,826,240-63,826,291 , GRCh37.p13 chr17: 61,903,600-61,903,651 , PSMC5, 1 more genes
    nsv5324239copy number variation1nstd204human GRCh38.p13 chr17: 63,820,670-63,823,947 , GRCh37.p13 chr17: 61,898,030-61,901,307 FTSJ3
    nsv5292062copy number variation1nstd204human GRCh38.p13 chr17: 63,540,501-63,873,300 , GRCh37.p13 chr17: 61,617,862-61,950,660 , KCNH6, 18 more genes
    nsv5282418copy number variation1nstd204human GRCh38.p13 chr17: 63,822,776-63,824,007 , GRCh37.p13 chr17: 61,900,136-61,901,367 FTSJ3
    nsv5281162copy number variation1nstd204human GRCh38.p13 chr17: 63,820,732-63,823,807 , GRCh37.p13 chr17: 61,898,092-61,901,167 FTSJ3
    nsv5157681mobile element insertion1nstd203human GRCh38 chr17: 63,826,226-63,826,240 , GRCh37.p13 chr17: 61,903,586-61,903,600 , PSMC5, 1 more genes
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