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Items: 1 to 20 of 340

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2786511copy number variation1nstd132human NCBI36 (hg18) chr9: 78,984,573-79,220,649 , GRCh37 (hg19) chr9: 79,794,753-80,030,829 , GRCh38 (hg38) chr9: 77,179,837-77,415,913 VPS13A
    nsv2783839copy number variation1nstd132human NCBI36 (hg18) chr9: 79,000,709-79,200,747 , GRCh37 (hg19) chr9: 79,810,889-80,010,927 , GRCh38 (hg38) chr9: 77,195,973-77,396,011 VPS13A
    nsv2783642copy number variation1nstd132human NCBI36 (hg18) chr9: 79,000,709-79,220,649 , GRCh37 (hg19) chr9: 79,810,889-80,030,829 , GRCh38 (hg38) chr9: 77,195,973-77,415,913 VPS13A
    nsv2774604copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 68,734,571-83,557,267 , GRCh38 (hg38) chr9: 40,915,719-80,942,352 , NCBI36 (hg18) chr9: 68,124,391-82,747,087 FAM27E3, FRG1HP, 96 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
    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
    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
    nsv2769481copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 70,966,262-90,761,254 , GRCh38 (hg38) chr9: 68,351,346-88,146,339 , NCBI36 (hg18) chr9: 70,156,082-89,951,074 VPS13A-AS1, GAS1RR, 90 more genes
    esv3857837copy number variation1estd219human GRCh37 (hg19) chr9: 79,858,105-79,859,821 , GRCh38 (hg38) chr9: 77,243,189-77,244,905 VPS13A
    esv3857836copy number variation2estd219human GRCh37 (hg19) chr9: 79,831,006-79,833,298 , GRCh38 (hg38) chr9: 77,216,090-77,218,382 VPS13A
    esv3857839copy number variation1estd219human GRCh37 (hg19) chr9: 79,999,148-80,016,577 , GRCh38 (hg38) chr9: 77,384,232-77,401,661 VPS13A
    esv3857838copy number variation1estd219human GRCh37 (hg19) chr9: 79,871,679-79,875,058 , GRCh38 (hg38) chr9: 77,256,763-77,260,142 VPS13A
    esv3857835copy number variation1estd219human GRCh37 (hg19) chr9: 79,801,592-79,843,851 , GRCh38 (hg38) chr9: 77,186,676-77,228,935 VPS13A
    esv3857840copy number variation1estd219human GRCh37 (hg19) chr9: 80,000,593-80,033,618 , GRCh38 (hg38) chr9: 77,385,677-77,418,702 VPS13A
    nsv2756841copy number variation1nstd130human GRCh37 (hg19) chr9: 502,292-140,777,105 , GRCh38 (hg38) chr9: 502,292-137,882,653 TRH-GTG1-6, FOXD4L2, 1023 more genes
    nsv2756711copy number variation2nstd130human GRCh37 (hg19) chr9: 79,939,592-80,032,108 , GRCh38 (hg38) chr9: 77,324,676-77,417,192 VPS13A
    nsv2745220copy number variation1nstd130human NCBI36 (hg18) chr9: 70,151,170-139,876,646 , GRCh37 (hg19) chr9: 71,130,848-140,756,825 , GRCh38 (hg38) chr9: 68,346,434-137,862,373 SNORA84, SNORA70C, 707 more genes
    nsv2735676copy number variation1nstd130human NCBI36 (hg18) chr9: 326,186-137,969,530 , GRCh37 (hg19) chr9: 336,186-138,829,709 , GRCh38 (hg38) chr9: 193,412-135,937,863 TRH-GTG1-6, FOXD4L2, 928 more genes
    nsv2735670copy number variation1nstd130human NCBI36 (hg18) chr9: 198,549-138,844,941 , GRCh37 (hg19) chr9: 208,549-139,725,120 , GRCh38 (hg38) chr9: 193,412-136,830,668 TRH-GTG1-6, FOXD4L2, 966 more genes
    nsv2625817short tandem repeat6nstd128human GRCh37 (hg19) chr9: 80,007,732-80,007,746 , GRCh38 (hg38) chr9: 77,392,816-77,392,830 VPS13A
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