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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3150209copy number variation1nstd151human GRCh37 (hg19) chr10: 46,611,714-46,611,816 , GRCh38 (hg38) chr10: 46,940,618-46,940,720 PTPN20, PTPN20A
    nsv3144346copy number variation2nstd151human GRCh37 (hg19) chr10: 46,242,046-47,416,979 , GRCh38 (hg38) chr10: 46,146,977-46,737,090 FAM25BP, CTSLP7, 10 more genes
    nsv3143765copy number variation1nstd151human GRCh37 (hg19) chr10: 46,248,034-47,158,901 , GRCh38 (hg38) chr10: 46,146,977-46,737,090 FAM25BP, ANTXRLP1, 8 more genes
    nsv3141969copy number variation2nstd151human GRCh37 (hg19) chr10: 46,282,058-46,928,014 , GRCh38 (hg38) chr10: 46,146,977-46,737,090 FAM25BP, ANTXRLP1, 8 more genes
    nsv3110279copy number variation1nstd145human GRCh37 (hg19) chr10: 46,221,053-47,703,200 , GRCh38 (hg38) chr10: 45,725,605-48,074,662 FAM25BP, FAM25G, 28 more genes
    nsv3109667copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr10: 45,502,266-51,581,091 , GRCh37 (hg19) chr10: 46,182,260-51,911,085 , GRCh38 (hg38) chr10: 45,686,812-50,151,325 FAM25BP, FAM25G, 58 more genes
    nsv2778356copy number variation19nstd37humanBenign NCBI36 (hg18) chr10: 45,970,853-47,010,400 , GRCh37 (hg19) chr10: 46,550,847-47,531,169 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 20 more genes
    nsv2777764copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 100,026-50,961,640 , GRCh38 (hg38) chr10: 54,086-49,753,594 , NCBI36 (hg18) chr10: 90,026-50,631,646 ABI1, MIR938, 335 more genes
    nsv2777424copy number variation1nstd37humanBenign NCBI36 (hg18) chr10: 45,970,853-46,581,391 , GRCh37 (hg19) chr10: 46,550,847-47,161,385 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 18 more genes
    nsv2777383copy number variation2nstd37humanBenign NCBI36 (hg18) chr10: 46,044,427-47,010,400 , GRCh37 (hg19) chr10: 46,624,421-47,531,169 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh38 (hg38) chr10: 46,146,977-47,923,579 FAM25BP, FAM25G, 19 more genes
    nsv2775917copy number variation1nstd37humanBenign NCBI36 (hg18) chr10: 45,725,327-47,124,910 , GRCh37.p13 chr10|NW_003871068.1: 180,988-2,010,264 , GRCh37 (hg19) chr10: 46,476,965-47,531,169 , GRCh38 (hg38) chr10: 45,909,873-48,074,662 FAM25BP, FAM25G, 24 more genes
    nsv2775746copy number variation1nstd37humanBenign NCBI36 (hg18) chr10: 45,953,420-46,578,690 , GRCh37 (hg19) chr10: 46,533,414-47,158,684 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 18 more genes
    nsv2775299copy number variation1nstd37humanBenign NCBI36 (hg18) chr10: 45,986,714-47,010,400 , GRCh37 (hg19) chr10: 46,566,708-47,531,169 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 20 more genes
    nsv2775048copy number variation1nstd37humanBenign GRCh37 (hg19) chr10: 46,491,169-46,550,969 , GRCh38 (hg38) chr10: 47,001,474-47,060,850 , NCBI36 (hg18) chr10: 45,911,175-45,970,975 PTPN20, PTPN20A
    nsv2773775copy number variation1nstd37humanBenign GRCh37 (hg19) chr10: 46,491,169-46,550,696 , GRCh38 (hg38) chr10: 47,001,747-47,060,850 , NCBI36 (hg18) chr10: 45,911,175-45,970,702 PTPN20, PTPN20A
    nsv2772290copy number variation4nstd37humanBenign NCBI36 (hg18) chr10: 45,970,853-47,189,902 , GRCh37 (hg19) chr10: 46,550,847-47,719,896 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 20 more genes
    nsv2771541copy number variation1nstd37humanBenign NCBI36 (hg18) chr10: 45,970,853-47,208,634 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh37 (hg19) chr10: 46,550,847-47,738,628 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 20 more genes
    nsv2771328copy number variation1nstd37humanLikely benign NCBI36 (hg18) chr10: 45,970,809-47,172,593 , GRCh37 (hg19) chr10: 46,550,803-47,702,587 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh38 (hg38) chr10: 46,146,977-48,074,662 FAM25BP, FAM25G, 20 more genes
    nsv2770979copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 46,224,446-51,594,991 , GRCh38 (hg38) chr10: 45,728,998-49,929,364 , NCBI36 (hg18) chr10: 45,544,452-51,264,997 FAM25BP, FAM25G, 54 more genes
    nsv2770825copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr10: 46,210,750-51,753,095 , GRCh38 (hg38) chr10: 45,715,302-49,993,335 , NCBI36 (hg18) chr10: 45,530,756-51,423,101 FAM25BP, FAM25G, 57 more genes
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