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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6991724copy number variation1nstd229human GRCh38 chr17: 42,780,061-42,789,521 , GRCh37.p13 chr17: 40,932,079-40,941,539 WNK4, VPS25
    nsv6985364copy number variation1nstd229human GRCh38 chr17: 42,723,977-42,924,183 , GRCh37.p13 chr17: 40,875,995-41,076,200 AOC2, WNK4, 15 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6510237copy number variation1nstd223human GRCh38 chr17: 42,789,474-42,791,359 , GRCh37.p13 chr17: 40,941,492-40,943,377 WNK4
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 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
    nsv5529978copy number variation1nstd206human GRCh38 chr17: 42,783,072-42,783,338 , GRCh37.p13 chr17: 40,935,090-40,935,356 WNK4
    nsv5520825copy number variation1nstd206human GRCh38 chr17: 42,789,355-42,791,449 , GRCh37.p13 chr17: 40,941,373-40,943,467 WNK4
    nsv5320781copy number variation1nstd204human GRCh38.p13 chr17: 42,789,446-42,791,374 , GRCh37.p13 chr17: 40,941,464-40,943,392 WNK4
    nsv5016446copy number variation1nstd200human GRCh38 chr17: 42,789,449-42,791,379 , GRCh37.p13 chr17: 40,941,467-40,943,397 WNK4
    nsv4858851copy number variation1nstd200human GRCh37 chr17: 40,933,307-40,933,359 , GRCh38.p12 chr17: 42,781,289-42,781,341 WNK4
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4267202copy number variation1nstd166human GRCh37.p13 chr17: 40,933,289-40,933,925 , GRCh38.p12 chr17: 42,781,271-42,781,907 WNK4
    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
    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
    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
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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