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Items: 1 to 20 of 114

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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
    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
    nsv6985713copy number variation1nstd229human GRCh38 chr17: 8,726,467-8,729,823 , GRCh37.p13 chr17: 8,629,785-8,633,141 CCDC42
    nsv6983528copy number variation1nstd229human GRCh38 chr17: 8,742,301-8,946,653 , GRCh37.p13 chr17: 8,645,619-8,849,970 PIK3R5, LOC105371530, 6 more genes
    nsv6133429copy number variation1nstd213human GRCh37 chr17: 8,440,000-9,870,001 , GRCh38.p12 chr17: 8,536,682-9,966,684 MYH10, RCVRN, 25 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
    nsv5653258insertion1nstd207human GRCh38 chr17: 8,728,171-8,728,171 , GRCh37.p13 chr17: 8,631,489-8,631,489 CCDC42
    nsv5525871copy number variation1nstd206human GRCh38 chr17: 8,734,324-8,734,421 , GRCh37.p13 chr17: 8,637,642-8,637,739 CCDC42
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4555587insertion2nstd166human GRCh37.p13 chr17: 8,631,420-8,631,420 , GRCh38.p12 chr17: 8,728,102-8,728,102 CCDC42
    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
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3902311copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,929,776-9,995,862 , GRCh38.p12 chr17: 8,026,458-10,092,545 RCVRN, TRQ-CTG1-5, 74 more genes
    nsv3901829copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,412,394-8,729,543 , GRCh38.p12 chr17: 8,509,076-8,826,226 MFSD6L, LOC102724262, 11 more genes
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