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Items: 1 to 20 of 27

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908797copy number variation1nstd102humanLikely benign GRCh37 chr17: 57,352,957-57,456,309 , GRCh38.p12 chr17: 59,275,596-59,378,948 YPEL2, MIR4729, 2 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 YPEL2, PRPSAP1, 1350 more genes
    nsv3895056copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,623,275-60,285,107 , GRCh38.p12 chr17: 58,545,914-62,207,746 YPEL2, MIR454, 87 more genes
    nsv3914957copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,496,167-57,812,825 , GRCh38 chr17: 57,418,806-59,735,464 , NCBI36 chr17: 52,851,166-55,167,607 YPEL2, CLTC, 67 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 YPEL2, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 YPEL2, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 YPEL2, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 YPEL2, 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 YPEL2, LOC105371922, 1855 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 YPEL2, FOXK2, 958 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 YPEL2, RNU6-131P, 1075 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 YPEL2, PLEKHH3, 958 more genes
    nsv3890268copy number variation1nstd102humanPathogenic GRCh37 chr17: 49,076,980-58,740,945 , GRCh38.p12 chr17: 50,999,619-60,663,584 YPEL2, NDUFB8P2, 161 more genes
    nsv4349383copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527 YPEL2, FAM136DP, 214 more genes
    nsv3895703copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,321,134-62,080,001 , GRCh38.p12 chr17: 58,243,773-64,002,641 YPEL2, GH2, 161 more genes
    nsv3892374copy number variation1nstd102humanPathogenic GRCh37 chr17: 52,189,051-57,477,162 , GRCh38.p12 chr17: 54,111,690-59,399,801 YPEL2, RN7SKP14, 93 more genes
    nsv6291758copy number variation1nstd102humanLikely benign GRCh37 chr17: 57,301,383-57,627,245 , GRCh38.p12 chr17: 59,224,022-59,549,884 YPEL2, GDPD1, 6 more genes
    nsv3908452copy number variation1nstd102humanBenign GRCh37 chr17: 57,404,213-57,647,861 , GRCh38.p12 chr17: 59,326,852-59,570,500 YPEL2, DHX40, 5 more genes
    nsv3890666copy number variation1nstd102humanBenign GRCh37 chr17: 57,239,628-57,459,574 , GRCh38.p12 chr17: 59,162,267-59,382,213 YPEL2, SMG8, 5 more genes
    nsv3916281copy number variation1nstd102humanLikely benign GRCh38 chr17: 59,151,705-59,547,602 , GRCh37 chr17: 57,229,066-57,624,963 , NCBI36 chr17: 54,583,848-54,979,745 YPEL2, LOC105371847, 11 more genes
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