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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5699043mobile element insertion1nstd211human GRCh38 chr17: 63,826,240-63,826,240 , GRCh37.p13 chr17: 61,903,600-61,903,600 , PSMC5, 1 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531754copy number variation1nstd206human GRCh38 chr17: 63,821,424-63,821,502 , GRCh37.p13 chr17: 61,898,784-61,898,862 FTSJ3
    nsv5424992mobile element insertion1nstd206human GRCh38 chr17: 63,826,240-63,826,291 , GRCh37.p13 chr17: 61,903,600-61,903,651 , PSMC5, 1 more genes
    nsv5324239copy number variation1nstd204human GRCh38.p13 chr17: 63,820,670-63,823,947 , GRCh37.p13 chr17: 61,898,030-61,901,307 FTSJ3
    nsv5292062copy number variation1nstd204human GRCh38.p13 chr17: 63,540,501-63,873,300 , GRCh37.p13 chr17: 61,617,862-61,950,660 , KCNH6, 18 more genes
    nsv5282418copy number variation1nstd204human GRCh38.p13 chr17: 63,822,776-63,824,007 , GRCh37.p13 chr17: 61,900,136-61,901,367 FTSJ3
    nsv5281162copy number variation1nstd204human GRCh38.p13 chr17: 63,820,732-63,823,807 , GRCh37.p13 chr17: 61,898,092-61,901,167 FTSJ3
    nsv5157681mobile element insertion1nstd203human GRCh38 chr17: 63,826,226-63,826,240 , GRCh37.p13 chr17: 61,903,586-61,903,600 , PSMC5, 1 more genes
    nsv5141969mobile element insertion1nstd203human GRCh38 chr17: 63,825,643-63,825,661 , GRCh37.p13 chr17: 61,903,003-61,903,021 FTSJ3, PSMC5
    nsv4506880mobile element insertion1nstd166human GRCh37.p13 chr17: 61,903,586-61,903,586 , GRCh38.p12 chr17: 63,826,226-63,826,226 , PSMC5, 1 more genes
    nsv4505176mobile element insertion1nstd166human GRCh37.p13 chr17: 61,903,003-61,903,003 , GRCh38.p12 chr17: 63,825,643-63,825,643 FTSJ3, PSMC5
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4349383copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527 FAM136DP, HELZ, 214 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
    nsv3916307copy number variation1nstd102humanUncertain significance GRCh38 chr17: 63,648,253-63,855,879 , GRCh37 chr17: 61,725,613-61,933,239 , NCBI36 chr17: 59,079,345-59,286,971 PSMC5, FTSJ3, 9 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
    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 RNU6-131P, ZNF652, 1075 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 PRPSAP1, CACNG1, 1350 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 PLEKHH3, CHCT1, 958 more genes
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