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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5653517insertion1nstd207human GRCh38 chr17: 27,526,044-27,526,044 , GRCh37.p13 chr17: 25,853,070-25,853,070 MSANTD3P1, KSR1
    nsv4858431copy number variation1nstd200human GRCh37 chr17: 25,851,279-25,851,364 , GRCh38.p12 chr17: 27,524,253-27,524,338 KSR1, MSANTD3P1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 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
    nsv4379025copy number variation1nstd173human GRCh37 chr17: 25,307,567-27,710,963 , GRCh38.p12 chr17: 26,980,541-29,383,945 , MIR451A, 91 more genes
    nsv4376928copy number variation1nstd173human GRCh37 chr17: 25,443,376-26,031,625 , GRCh38.p12 chr17: 27,116,350-27,704,599 NOS2P1, KSR1, 13 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
    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
    nsv3923666copy number variation1nstd102humanUncertain significance NCBI36 chr17: 22,367,302-22,879,117 , GRCh37 chr17: 25,343,175-25,854,990 , GRCh38 chr17: 27,016,149-27,527,964 WSB1, LOC105371704, 12 more genes
    nsv3919964copy number variation1nstd102humanUncertain significance NCBI36 chr17: 22,715,228-22,934,320 , GRCh37.p13 chr17: 25,691,101-25,910,193 , GRCh38.p12 chr17: 27,364,075-27,583,167 TBC1D3P5, KSR1, 2 more genes
    nsv3915019copy number variation1nstd102humanLikely benign GRCh37 chr17: 25,291,809-25,910,253 , NCBI36 chr17: 22,315,936-22,934,380 , GRCh38 chr17: 26,964,783-27,583,227 MSANTD3P1, RPS16P8, 14 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
    nsv3908058copy number variation1nstd102humanLikely benign GRCh37 chr17: 25,545,321-25,860,210 , GRCh38.p12 chr17: 27,218,295-27,533,184 SYPL1P2, WSB1, 8 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3904523copy number variation1nstd102humanLikely benign GRCh37 chr17: 25,270,398-26,075,070 , GRCh38.p12 chr17: 26,943,372-27,748,044 TUFMP1, LOC100422478, 20 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3903658copy number variation1nstd102humandrug response GRCh37 chr17: 25,248,166-30,645,676 , GRCh38.p12 chr17: 26,935,981-32,318,657 KRT18P55, CPDP1, 179 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
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