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Items: 1 to 20 of 491

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2819635copy number variation1nstd137human GRCh38 (hg38) chr9: 14,861,175-14,861,292 , GRCh37 (hg19) chr9: 14,861,173-14,861,290 FREM1
    nsv2819634insertion1nstd137human GRCh38 (hg38) chr9: 14,778,721-14,778,721 , GRCh37 (hg19) chr9: 14,778,719-14,778,719 FREM1
    nsv2818745copy number variation1nstd137human GRCh38 (hg38) chr9: 14,860,783-14,860,866 , GRCh37 (hg19) chr9: 14,860,781-14,860,864 FREM1
    nsv2777670copy number variation1nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,161,607 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,356,871 TRH-GTG1-6, CDKN2B-AS1, 307 more genes
    nsv2777580copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 4,581,369-14,848,338 , GRCh38 (hg38) chr9: 4,581,369-14,848,340 , NCBI36 (hg18) chr9: 4,571,369-14,838,338 TRH-GTG1-6, LINC00583, 42 more genes
    nsv2777269copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-38,787,480 , GRCh38 (hg38) chr9: 203,861-38,787,483 , NCBI36 (hg18) chr9: 193,861-38,777,480 TRH-GTG1-6, CDKN2B-AS1, 260 more genes
    nsv2776570copy number variation3nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,238,530 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,433,794 TRH-GTG1-6, CDKN2B-AS1, 307 more genes
    nsv2775336copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-67,983,174 , GRCh38 (hg38) chr9: 203,861-68,257,015 , NCBI36 (hg18) chr9: 193,861-67,572,994 TRH-GTG1-6, FOXD4L2, 313 more genes
    nsv2775104copy number variation1nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,250,706 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,445,970 TRH-GTG1-6, CDKN2B-AS1, 307 more genes
    nsv2774988copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-16,670,878 , GRCh38 (hg38) chr9: 203,861-16,670,880 , NCBI36 (hg18) chr9: 193,861-16,660,878 TRH-GTG1-6, LINC00583, 68 more genes
    nsv2774488copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr9: 2,934-140,273,252 , GRCh37 (hg19) chr9: 12,934-141,153,431 , GRCh38 (hg38) chr9: 12,934-138,262,981 TRH-GTG1-6, FOXD4L2, 1035 more genes
    nsv2773829copy number variation2nstd37humanBenign NCBI36 (hg18) chr9: 47,102,101-70,129,166 , GRCh37 (hg19) chr9: 47,312,281-70,871,931 , GRCh38 (hg38) chr9: 193,412-68,324,430 TRH-GTG1-6, CDKN2B-AS1, 305 more genes
    nsv2773768copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-69,002,883 , GRCh38 (hg38) chr9: 203,861-68,257,015 , NCBI36 (hg18) chr9: 193,861-68,292,703 TRH-GTG1-6, FOXD4L2, 314 more genes
    nsv2773513copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-88,189,913 , GRCh38 (hg38) chr9: 203,861-85,574,998 , NCBI36 (hg18) chr9: 193,861-87,379,733 TRH-GTG1-6, FOXD4L2, 393 more genes
    nsv2773404copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-15,211,277 , GRCh38 (hg38) chr9: 203,861-15,211,279 , NCBI36 (hg18) chr9: 193,861-15,201,277 TRH-GTG1-6, LINC00583, 62 more genes
    nsv2773152copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,864-141,020,389 , GRCh38 (hg38) chr9: 203,864-138,125,937 , NCBI36 (hg18) chr9: 193,864-140,140,210 TRH-GTG1-6, FOXD4L2, 1025 more genes
    nsv2772450copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-68,188,391 , GRCh38 (hg38) chr9: 203,861-68,257,015 , NCBI36 (hg18) chr9: 193,861-67,678,211 TRH-GTG1-6, FOXD4L2, 313 more genes
    nsv2772408copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-17,655,298 , GRCh38 (hg38) chr9: 203,861-17,655,300 , NCBI36 (hg18) chr9: 193,861-17,645,298 TRH-GTG1-6, LINC00583, 70 more genes
    nsv2771898copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 32,396-39,140,211 , GRCh38 (hg38) chr9: 32,396-39,140,214 , NCBI36 (hg18) chr9: 22,396-39,130,211 TRH-GTG1-6, CDKN2B-AS1, 267 more genes
    nsv2771726copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr9: 2,934-65,222,364 , GRCh37 (hg19) chr9: 12,934-65,482,544 , GRCh38 (hg38) chr9: 12,934-67,217,006 TRH-GTG1-6, FOXD4L2, 318 more genes
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