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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5670947inversion1nstd207human GRCh38 chr13: 52,344,011-52,502,256 , GRCh37.p13 chr13: 52,918,146-53,076,391 CKAP2, VPS36, 5 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5547165insertion1nstd206human GRCh38 chr13: 52,376,733-52,376,794 , GRCh37.p13 chr13: 52,950,868-52,950,929 THSD1
    nsv5508258copy number variation1nstd206human GRCh38 chr13: 52,362,043-52,377,211 , GRCh37.p13 chr13: 52,936,178-52,951,346 THSD1
    nsv5356899translocation1nstd200human GRCh38 chr13: 52,376,794-52,376,794 , GRCh38 chr13: 52,167,391-52,167,391 , GRCh37.p13 chr13: 52,741,526-52,741,526 , GRCh37.p13 chr13: 52,950,929-52,950,929 THSD1, THSD1P1, 1 more genes
    nsv5345806translocation1nstd200human GRCh37 chr13: 52,950,929-52,950,929 , GRCh37 chr13: 52,741,526-52,741,526 , GRCh38.p12 chr13: 52,167,391-52,167,391 , GRCh38.p12 chr13: 52,376,794-52,376,794 THSD1, THSD1P1, 1 more genes
    nsv5302169copy number variation1nstd204human GRCh38.p13 chr13: 52,394,492-52,394,943 , GRCh37.p13 chr13: 52,968,627-52,969,078 THSD1
    nsv5264676copy number variation1nstd204human GRCh38.p13 chr13: 52,339,366-52,378,626 , GRCh37.p13 chr13: 52,913,501-52,952,761 LINC02333, THSD1, 1 more genes
    nsv5158692mobile element insertion1nstd203human GRCh38 chr13: 52,401,288-52,401,299 , GRCh37.p13 chr13: 52,975,423-52,975,434 THSD1
    nsv5006494copy number variation1nstd200human GRCh38 chr13: 52,389,695-52,389,785 , GRCh37.p13 chr13: 52,963,830-52,963,920 THSD1
    nsv5006493copy number variation1nstd200human GRCh38 chr13: 52,383,732-52,386,919 , GRCh37.p13 chr13: 52,957,867-52,961,054 THSD1
    nsv5006491copy number variation1nstd200human GRCh38 chr13: 52,362,012-52,377,240 , GRCh37.p13 chr13: 52,936,147-52,951,375 THSD1
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4842054copy number variation1nstd200human GRCh37 chr13: 52,968,637-52,969,069 , GRCh38.p12 chr13: 52,394,502-52,394,934 THSD1
    nsv4835409copy number variation1nstd200human GRCh37 chr13: 52,957,867-52,961,054 , GRCh38.p12 chr13: 52,383,732-52,386,919 THSD1
    nsv4769378copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,170,957-57,713,087 , GRCh38.p12 chr13: 51,596,821-57,138,953 CTAGE3P, TMEM272, 46 more genes
    nsv4732557copy number variation1nstd199human GRCh37 chr13: 52,963,998-52,964,258 , GRCh38.p12 chr13: 52,389,863-52,390,123 THSD1
    nsv4730069inversion4nstd198human GRCh38 chr13: 52,209,770-52,601,273 , GRCh37.p13 chr13: 52,783,905-53,175,408 CKAP2, VPS36, 7 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4538636insertion1nstd166human GRCh37.p13 chr13: 52,949,399-52,949,399 , GRCh38.p12 chr13: 52,375,264-52,375,264 THSD1
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