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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130630insertion1nstd186human GRCh37 chr17: 41,910,641-41,910,649 , GRCh38.p12 chr17: 43,833,273-43,833,281 MPP3, LOC107984979
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5545925insertion1nstd206human GRCh38 chr17: 43,833,273-43,833,281 , GRCh37.p13 chr17: 41,910,641-41,910,649 MPP3, LOC107984979
    nsv5016492copy number variation1nstd200human GRCh38 chr17: 43,807,119-43,811,857 , GRCh37.p13 chr17: 41,884,487-41,889,225 MPP3
    nsv4680708copy number variation1nstd189human GRCh37.p13 chr17: 41,357,686-42,167,307 , GRCh38.p12 chr17: 43,205,667-44,089,939 , ARL4D, 41 more genes
    nsv4674980copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-42,125,780 , GRCh38.p12 chr17: 43,322,528-44,048,412 RPL29P31, MEOX1, 34 more genes
    nsv4457523copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,800,157-41,903,109 , GRCh38.p12 chr17: 43,722,789-43,825,741 MPP3, CFAP97D1, 2 more genes
    nsv4368311copy number variation1nstd173human GRCh37 chr17: 41,384,516-42,395,351 , GRCh38.p12 chr17: 43,307,154-44,317,983 , LOC105371789, 55 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
    nsv4252982copy number variation1nstd166human GRCh37.p13 chr17: 41,884,487-41,889,225 , GRCh38.p12 chr17: 43,807,119-43,811,857 MPP3
    nsv3968682copy number variation1nstd168human GRCh38 chr17: 43,796,206-43,826,585 , GRCh37.p13 chr17: 41,873,574-41,903,953 MPP3
    nsv3923117copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,080,123-43,897,875 , NCBI36 chr17: 38,485,666-39,330,769 , GRCh37 chr17: 41,232,140-41,975,243 RNU6-470P, CCDC200, 33 more genes
    nsv3922353copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,088,882-43,865,172 , GRCh37 chr17: 41,240,899-41,942,540 , NCBI36 chr17: 38,494,425-39,298,066 NBR1, LOC107985077, 31 more genes
    nsv3921716copy number variation1nstd102humanUncertain significance NCBI36 chr17: 38,456,488-39,330,777 , GRCh38 chr17: 43,050,945-43,897,883 , GRCh37 chr17: 41,202,962-41,975,251 LINC02594, MEOX1, 33 more genes
    nsv3920812copy number variation1nstd102humanLikely benign GRCh38 chr17: 43,322,528-43,849,385 , NCBI36 chr17: 38,755,418-39,282,279 , GRCh37 chr17: 41,399,892-41,926,753 MEOX1, LINC02594, 22 more genes
    nsv3919609copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,648,246-42,839,745 , GRCh38 chr17: 43,570,878-44,762,377 , NCBI36 chr17: 39,003,772-40,195,271 SMCO4P1, LINC01180, 59 more genes
    nsv3918675copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,387,123-43,865,083 , NCBI36 chr17: 38,820,017-39,297,977 , GRCh37 chr17: 41,464,491-41,942,451 ARL4D, LOC107984979, 21 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
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