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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6993676copy number variation1nstd229human GRCh38 chr17: 33,729,995-34,320,708 , GRCh37.p13 chr17: 32,057,014-32,647,727 CCL8, LOC105371735, 11 more genes
    nsv6985764copy number variation1nstd229human GRCh38 chr17: 33,829,201-34,469,400 , GRCh37.p13 chr17: 32,156,220-32,796,419 TLK2P1, LOC105371735, 13 more genes
    nsv6983076copy number variation1nstd229human GRCh38 chr17: 33,829,301-34,469,500 , GRCh37.p13 chr17: 32,156,320-32,796,519 CCL8, LOC105371735, 13 more genes
    nsv6980794copy number variation1nstd229human GRCh38 chr17: 33,631,491-34,610,756 , GRCh37.p13 chr17: 31,958,510-32,937,775 LOC107985036, ASIC2, 17 more genes
    nsv6979965copy number variation1nstd229human GRCh38 chr17: 33,774,328-34,498,680 , GRCh37.p13 chr17: 32,101,347-32,825,699 CCL7, LINC01989, 15 more genes
    nsv6624071copy number variation1nstd224human GRCh37 chr17: 31,960,248-32,930,312 , GRCh38.p12 chr17: 33,633,229-34,603,293 ASIC2, CCL2, 17 more genes
    nsv6498266copy number variation1nstd223human GRCh38 chr17: 33,631,491-34,610,756 , GRCh37.p13 chr17: 31,958,510-32,937,775 CCL8, LOC105371738, 17 more genes
    nsv6314149copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,959,226-32,937,658 , GRCh38.p12 chr17: 33,632,207-34,610,639 LOC105371735, TLK2P1, 17 more genes
    nsv6133303copy number variation1nstd213human GRCh37 chr17: 32,450,000-32,710,001 , GRCh38.p12 chr17: 34,122,981-34,382,982 ASIC2, CCL1, 7 more genes
    nsv6133240copy number variation1nstd213human GRCh37 chr17: 31,450,000-32,700,001 , GRCh38.p12 chr17: 33,122,982-34,372,982 CCL2, LOC147004, 17 more genes
    nsv6133239copy number variation1nstd213human GRCh37 chr17: 31,430,000-33,140,001 , GRCh38.p12 chr17: 33,102,982-34,812,982 ASIC2, CCL1, 23 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
    nsv5029040copy number variation1nstd200human GRCh38 chr17: 33,729,995-34,320,708 , GRCh37.p13 chr17: 32,057,014-32,647,727 , LOC107985038, 12 more genes
    nsv5029039copy number variation1nstd200human GRCh38 chr17: 33,631,491-34,610,756 , GRCh37.p13 chr17: 31,958,510-32,937,775 , TLK2P1, 18 more genes
    nsv4864615copy number variation1nstd200human GRCh37 chr17: 32,057,014-32,647,727 , GRCh38.p12 chr17: 33,729,995-34,320,708 , LOC107987247, 12 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4621313copy number variation1nstd183human GRCh37 chr17: 31,959,395-32,938,034 , GRCh38.p12 chr17: 33,632,376-34,611,015 , LOC105371735, 18 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
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