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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066785inversion1nstd229human GRCh38 chr17: 48,650,784-48,769,648 , GRCh37.p13 chr17: 46,728,146-46,847,010 TTLL6, LOC105371812, 9 more genes
    nsv6637543copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,753,824-47,577,721 , GRCh38.p12 chr17: 48,676,462-49,500,359 CALCOCO2, SUMO2P17, 37 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
    nsv5381107copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,804,152-46,804,415 , GRCh38.p12 chr17: 48,726,790-48,727,053 HOXB13
    nsv5026313copy number variation1nstd200human GRCh38 chr17: 48,721,867-48,751,113 , GRCh37.p13 chr17: 46,799,229-46,828,475 HOXB13, PRAC1, 4 more genes
    nsv5013785copy number variation1nstd200human GRCh38 chr17: 48,719,127-49,313,149 , GRCh37.p13 chr17: 46,796,489-47,390,511 , UBE2Z, 30 more genes
    nsv5013784copy number variation1nstd200human GRCh38 chr17: 48,704,646-48,922,409 , GRCh37.p13 chr17: 46,782,008-46,999,771 SUMO2P17, HOXB13, 15 more genes
    nsv4867211copy number variation1nstd200human GRCh37 chr17: 46,799,229-46,828,475 , GRCh38.p12 chr17: 48,721,867-48,751,113 HOXB13, PRAC1, 4 more genes
    nsv4682729copy number variation2nstd102humanUncertain significance GRCh37 chr17: 46,804,152-46,805,955 , GRCh38.p12 chr17: 48,726,790-48,728,593 HOXB13
    nsv4503053mobile element insertion1nstd166human GRCh37.p13 chr17: 46,806,581-46,806,581 , GRCh38.p12 chr17: 48,729,219-48,729,219 HOXB13
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4024330mobile element insertion1nstd166human GRCh37.p13 chr17: 46,806,596-46,806,596 , GRCh38.p12 chr17: 48,729,234-48,729,234 HOXB13
    nsv3920056copy number variation1nstd102humanUncertain significance NCBI36 chr17: 43,882,989-44,985,282 , GRCh38 chr17: 48,450,628-49,552,921 , GRCh37 chr17: 46,527,990-47,630,283 ZNF652-AS1, RPS10P25, 55 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3913486copy number variation1nstd102humanPathogenic GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570 MIR6165, NGFR, 54 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911757copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,419,251-44,761,758 , GRCh37 chr17: 46,064,252-47,406,759 , GRCh38 chr17: 47,986,886-49,329,397 LINC02086, RNU6-1152P, 59 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
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