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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7146843insertion1nstd232human GRCh37.p13 chr17: 8,408,227-8,408,227 , GRCh38.p12 chr17: 8,504,909-8,504,909 MYH10, LOC102724262
    nsv7145881insertion1nstd232human GRCh37.p13 chr17: 8,413,268-8,413,268 , GRCh38.p12 chr17: 8,509,950-8,509,950 MYH10, RNU7-43P, 1 more genes
    nsv7142984copy number variation1nstd232human GRCh37.p13 chr17: 8,416,983-8,417,098 , GRCh38.p12 chr17: 8,513,665-8,513,780 MYH10, LOC102724262
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    nsv6511624copy number variation1nstd223human GRCh38 chr17: 8,510,330-8,512,300 , GRCh37.p13 chr17: 8,413,648-8,415,618 MYH10, RNU7-43P, 1 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv6088434insertion1nstd212human GRCh38 chr17: 8,511,029-8,511,029 , GRCh37.p13 chr17: 8,414,347-8,414,347 MYH10, RNU7-43P, 1 more genes
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5536596insertion1nstd206human GRCh38 chr17: 8,511,062-8,511,084 , GRCh37.p13 chr17: 8,414,380-8,414,402 MYH10, RNU7-43P, 1 more genes
    nsv4768106insertion1nstd199human GRCh37 chr17: 8,414,330-8,414,330 , GRCh38.p12 chr17: 8,511,012-8,511,012 MYH10, RNU7-43P, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv3937634copy number variation1nstd167human GRCh37 chr17: 8,414,333-8,414,363 , GRCh38.p12 chr17: 8,511,015-8,511,045 MYH10, RNU7-43P, 1 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 SLC2A4, CCDC92B, 401 more genes
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