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Items: 1 to 20 of 103

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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
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6985366copy number variation1nstd229human GRCh38 chr17: 32,217,501-32,374,500 , GRCh37.p13 chr17: 30,544,520-30,701,519 LOC105371731, ZNF207, 6 more genes
    nsv6576677inversion1nstd223human GRCh38 chr17: 32,349,005-32,349,527 , GRCh37.p13 chr17: 30,676,024-30,676,546 ZNF207, C17orf75, 1 more genes
    nsv6133300copy number variation1nstd213human GRCh37 chr17: 30,620,000-31,340,001 , GRCh38.p12 chr17: 32,292,981-33,012,983 ASIC2, MYO1D, 13 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133047copy number variation1nstd213human GRCh37 chr17: 30,150,000-30,710,001 , GRCh38.p12 chr17: 31,822,981-32,382,982 SH3GL1P1, ZNF207, 16 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
    nsv5016049copy number variation1nstd200human GRCh38 chr17: 32,348,114-32,348,836 , GRCh37.p13 chr17: 30,675,133-30,675,855 ZNF207, C17orf75, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729951copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,989,741-32,355,632 , GRCh38.p12 chr17: 31,662,722-34,028,613 RNA5SP437, PSMD11, 34 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
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4234046copy number variation1nstd166human GRCh37.p13 chr17: 30,657,307-33,838,598 , GRCh38.p12 chr17: 32,330,288-35,511,579 , PSMD11, 65 more genes
    nsv3972367copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446 ASIC2, AK4P1, 190 more genes
    nsv3958522copy number variation1nstd168human GRCh38 chr17: 32,341,821-32,355,976 , GRCh37.p13 chr17: 30,668,840-30,682,995 ZNF207, MIR632, 2 more genes
    nsv3919950copy number variation1nstd102humanPathogenic NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020 MIR365B, EFCAB5, 105 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
    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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