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Items: 1 to 20 of 539

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143480copy number variation1nstd232human GRCh37.p13 chr16: 88,871,073-88,871,166 , GRCh38.p12 chr16: 88,804,665-88,804,758 CDT1
    nsv7137571copy number variation1nstd232human GRCh37.p13 chr16: 88,873,610-88,873,686 , GRCh38.p12 chr16: 88,807,202-88,807,278 CDT1
    nsv7098789copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,870,240-88,878,307 , GRCh38.p12 chr16: 88,803,832-88,811,899 CDT1, APRT, 1 more genes
    nsv7095112copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,870,240-89,484,776 , GRCh38.p12 chr16: 88,803,832-89,418,368 LOC101927793, LOC105371409, 21 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7076684inversion1nstd229human GRCh38 chr16: 88,596,668-89,175,422 , GRCh37.p13 chr16: 88,663,076-89,241,830 LOC102724632, MIR4722, 28 more genes
    nsv6996623copy number variation1nstd229human GRCh38 chr16: 88,798,119-88,869,845 , GRCh37.p13 chr16: 88,864,527-88,936,253 GALNS, TRAPPC2L, 4 more genes
    nsv6990396copy number variation1nstd229human GRCh38 chr16: 88,756,075-88,821,570 , GRCh37.p13 chr16: 88,822,483-88,887,978 CDT1, GALNS, 2 more genes
    nsv6989464copy number variation1nstd229human GRCh38 chr16: 88,805,833-88,808,488 , GRCh37.p13 chr16: 88,872,241-88,874,896 APRT, CDT1
    nsv6982988copy number variation1nstd229human GRCh38 chr16: 88,809,552-89,123,925 , GRCh37.p13 chr16: 88,875,960-89,190,333 TRAPPC2L, CDT1, 13 more genes
    nsv6982878copy number variation1nstd229human GRCh38 chr16: 88,793,529-88,831,959 , GRCh37.p13 chr16: 88,859,937-88,898,367 GALNS, APRT, 1 more genes
    nsv6981140copy number variation1nstd229human GRCh38 chr16: 88,746,102-88,896,171 , GRCh37.p13 chr16: 88,812,510-88,962,579 PIEZO1, CBFA2T3, 8 more genes
    nsv6979954copy number variation1nstd229human GRCh38 chr16: 88,722,265-88,891,400 , GRCh37.p13 chr16: 88,788,673-88,957,808 GALNS, PABPN1L, 9 more genes
    nsv6979703copy number variation1nstd229human GRCh38 chr16: 88,192,059-88,802,307 , GRCh37.p13 chr16: 88,225,665-88,868,715 SNAI3, SNAI3-AS1, 20 more genes
    nsv6979129copy number variation1nstd229human GRCh38 chr16: 88,706,617-88,904,145 , GRCh37.p13 chr16: 88,773,025-88,970,553 LOC102724632, MIR4722, 13 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6624182copy number variation1nstd224human GRCh37 chr16: 88,358,766-89,261,442 , GRCh38.p12 chr16: 88,325,160-89,195,034 CDH15, CDT1, 36 more genes
    nsv6623797copy number variation1nstd224human GRCh37 chr16: 88,813,275-89,293,271 , GRCh38.p12 chr16: 88,746,867-89,226,863 APRT, PIEZO1, 19 more genes
    nsv6507687copy number variation1nstd223human GRCh38 chr16: 88,756,075-88,821,570 , GRCh37.p13 chr16: 88,822,483-88,887,978 PIEZO1, CDT1, 2 more genes
    nsv6504659copy number variation1nstd223human GRCh38 chr16: 88,770,801-88,862,200 , GRCh37.p13 chr16: 88,837,209-88,928,608 APRT, GALNS, 5 more genes
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