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Items: 1 to 20 of 23

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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 SLFN13, PSMD11, 117 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 SLFN13, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 SLFN13, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 SLFN13, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SLFN13, 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 SLFN13, LOC105371922, 1855 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 SLFN13, LOC105371753, 474 more genes
    nsv3908251copy number variation1nstd102humanBenign GRCh37 chr17: 33,680,811-33,768,199 , GRCh38.p12 chr17: 35,353,792-35,441,180 SLFN13, SLFN12, 4 more genes
    nsv3894181copy number variation1nstd102humanBenign GRCh37 chr17: 33,684,035-33,768,334 , GRCh38.p12 chr17: 35,357,016-35,441,315 SLFN13, SLFN12, 4 more genes
    nsv3895001copy number variation1nstd102humanBenign/Likely benign GRCh37 chr17: 33,687,356-33,767,930 , GRCh38.p12 chr17: 35,360,337-35,440,911 SLFN13, SLFN12, 4 more genes
    nsv3896708copy number variation1nstd102humanBenign GRCh37 chr17: 33,690,466-33,768,354 , GRCh38.p12 chr17: 35,363,447-35,441,335 SLFN13, SLFN12, 4 more genes
    nsv3897770copy number variation1nstd102humanLikely benign GRCh37 chr17: 33,498,726-33,863,479 , GRCh38.p12 chr17: 35,171,707-35,536,460 SLFN13, SLFN12L, 15 more genes
    nsv3898034copy number variation2nstd102humanBenign GRCh37 chr17: 33,684,035-33,768,199 , GRCh38.p12 chr17: 35,357,016-35,441,180 SLFN13, LOC105371933, 4 more genes
    nsv3908528copy number variation1nstd102humanBenign GRCh37 chr17: 33,691,903-33,768,199 , GRCh38.p12 chr17: 35,364,884-35,441,180 SLFN13, SLFN12, 4 more genes
    nsv3876148copy number variation3nstd102humannot provided GRCh37 chr17: 33,684,035-33,768,199 , GRCh38 chr17: 35,357,016-35,441,180 SLFN13, LOC729839, 4 more genes
    nsv3907376copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248 SLFN13, CCL8, 67 more genes
    nsv4675860copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,073,917-33,863,479 , GRCh38.p12 chr17: 34,746,898-35,536,460 SLFN13, RPL37P22, 26 more genes
    nsv3914031copy number variation1nstd102humanUncertain significance NCBI36 chr17: 30,480,991-31,118,181 , GRCh38 chr17: 35,129,859-35,767,049 , GRCh37 chr17: 33,456,878-34,094,068 SLFN13, UFM1P2, 30 more genes
    nsv7095147copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850 SLFN13, SLC35G3, 26 more genes
    nsv6634448copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,756,756-34,005,513 , GRCh38.p12 chr17: 35,429,737-35,678,494 SLFN13, LOC100420062, 13 more genes
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