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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682988copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr17: 63,526,094-63,554,738 , GRCh38.p12 chr17: 65,529,976-65,558,620 AXIN2
    nsv6310331copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,531,734-63,554,738 , GRCh38.p12 chr17: 65,535,616-65,558,620 AXIN2
    nsv7095411copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,534,311-63,537,685 , GRCh38.p12 chr17: 65,538,193-65,541,567 AXIN2
    nsv3882315copy number variation1nstd102humanPathogenic GRCh38 chr17: 65,536,314-65,536,559 , GRCh37 chr17: 63,532,432-63,532,677 AXIN2
    nsv5672866copy number variation1nstd102humanPathogenic GRCh38 chr17: 65,557,904-65,558,042 , GRCh37 chr17: 63,554,022-63,554,160 AXIN2
    nsv3870475copy number variation1nstd45humanPathogenic GRCh37 chr17: 63,524,681-63,557,740 , GRCh38.p12 chr17: 65,528,563-65,561,622 AXIN2
    nsv3873956copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 63,524,709-63,545,778 , GRCh38 chr17: 65,528,591-65,549,660 AXIN2
    nsv6310187copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,529,041-63,531,806 , GRCh38.p12 chr17: 65,532,923-65,535,688 AXIN2
    nsv6310402copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,526,094-63,526,230 , GRCh38.p12 chr17: 65,529,976-65,530,112 AXIN2
    nsv7093125copy number variation1nstd102humanUncertain significance GRCh38 chr17: 65,533,815-65,533,906 , GRCh37 chr17: 63,529,933-63,530,024 AXIN2
    nsv3879275copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,526,088-63,554,744 , GRCh38 chr17: 65,529,970-65,558,626 AXIN2
    nsv7095358copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,545,628-63,554,738 , GRCh38.p12 chr17: 65,549,510-65,558,620 AXIN2
    nsv6310403copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,526,094-63,530,207 , GRCh38.p12 chr17: 65,529,976-65,534,089 AXIN2
    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 AXIN2, PRPSAP1, 1350 more genes
    nsv3914737copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,649,313-65,683,004 , NCBI36 chr17: 60,061,351-63,113,466 , GRCh38 chr17: 64,634,771-67,686,888 AXIN2, RNU7-115P, 53 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 AXIN2, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 AXIN2, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 AXIN2, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 AXIN2, SMURF2, 2366 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 AXIN2, LOC105371922, 1855 more genes
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