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Items: 1 to 20 of 33

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4685778copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,119,174-57,128,690 , GRCh38.p12 chr17: 59,041,813-59,051,329 TRIM37
    nsv6310184copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,119,154-57,119,279 , GRCh38.p12 chr17: 59,041,793-59,041,918 TRIM37
    nsv7094908copy number variation1nstd102humanUncertain significance GRCh37 chr17: 57,076,738-57,094,805 , GRCh38.p12 chr17: 58,999,377-59,017,444 TRIM37
    nsv7094983copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,119,154-57,148,328 , GRCh38.p12 chr17: 59,041,793-59,070,967 TRIM37, RN7SL716P
    nsv3905500copy number variation1nstd102humanLikely benign GRCh37 chr17: 57,061,085-57,134,239 , GRCh38.p12 chr17: 58,983,724-59,056,878 TRIM37, PPM1E
    nsv3911607copy number variation1nstd102humanLikely benign NCBI36 chr17: 54,372,659-54,440,892 , GRCh37 chr17: 57,017,877-57,086,110 , GRCh38 chr17: 58,940,516-59,008,749 TRIM37, PPM1E
    nsv3895321copy number variation1nstd102humanLikely benign GRCh37 chr17: 56,998,237-57,064,254 , GRCh38.p12 chr17: 58,920,876-58,986,893 TRIM37, PPM1E
    nsv3901299copy number variation1nstd102humanBenign GRCh37 chr17: 56,854,249-57,177,549 , GRCh38.p12 chr17: 58,776,888-59,100,188 TRIM37, RNU6-518P, 3 more genes
    nsv3910705copy number variation1nstd102humanUncertain significance NCBI36 chr17: 54,400,326-54,533,437 , GRCh37.p13 chr17: 57,045,544-57,178,655 , GRCh38.p12 chr17: 58,968,183-59,101,294 TRIM37, RN7SL716P, 1 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 TRIM37, PRPSAP1, 1350 more genes
    nsv3895056copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,623,275-60,285,107 , GRCh38.p12 chr17: 58,545,914-62,207,746 TRIM37, 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 TRIM37, CLTC, 67 more genes
    nsv4684357copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,780,562-57,251,609 , GRCh38.p12 chr17: 58,703,201-59,174,248 TRIM37, SPDYE22P, 11 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 TRIM37, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 TRIM37, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 TRIM37, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 TRIM37, 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 TRIM37, LOC105371922, 1855 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 TRIM37, 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 TRIM37, RNU6-131P, 1075 more genes
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