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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7060867inversion1nstd229human GRCh38 chr17: 75,477,003-75,509,123 , GRCh37.p13 chr17: 73,473,084-73,505,204 TMEM94, CASKIN2, 1 more genes
    nsv6993778copy number variation1nstd229human GRCh38 chr17: 75,458,187-75,461,812 , GRCh37.p13 chr17: 73,454,268-73,457,893 TMEM94
    nsv6991297copy number variation1nstd229human GRCh38 chr17: 75,491,201-75,503,200 , GRCh37.p13 chr17: 73,487,282-73,499,281 MIR6785, TMEM94, 1 more genes
    nsv6990520copy number variation1nstd229human GRCh38 chr17: 75,442,198-75,485,045 , GRCh37.p13 chr17: 73,438,279-73,481,126 TMEM94
    nsv6989527copy number variation1nstd229human GRCh38 chr17: 75,491,247-75,491,276 , GRCh37.p13 chr17: 73,487,328-73,487,357 TMEM94
    nsv6988275copy number variation1nstd229human GRCh38 chr17: 75,458,683-75,469,995 , GRCh37.p13 chr17: 73,454,764-73,466,076 TMEM94
    nsv6986820copy number variation1nstd229human GRCh38 chr17: 75,448,925-75,455,683 , GRCh37.p13 chr17: 73,445,006-73,451,764 TMEM94
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983024copy number variation1nstd229human GRCh38 chr17: 75,494,709-75,505,079 , GRCh37.p13 chr17: 73,490,790-73,501,160 CASKIN2, TMEM94, 1 more genes
    nsv6978925copy number variation1nstd229human GRCh38 chr17: 75,457,340-75,461,033 , GRCh37.p13 chr17: 73,453,421-73,457,114 TMEM94
    nsv6978422copy number variation1nstd229human GRCh38 chr17: 75,423,467-75,460,638 , GRCh37.p13 chr17: 73,419,548-73,456,719 TMEM94
    nsv6592378inversion1nstd223human GRCh38 chr17: 75,461,812-75,462,121 , GRCh37.p13 chr17: 73,457,893-73,458,202 TMEM94
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6534969copy number variation1nstd223human GRCh38 chr17: 75,449,501-75,451,300 , GRCh37.p13 chr17: 73,445,582-73,447,381 TMEM94
    nsv6525732copy number variation1nstd223human GRCh38 chr17: 75,441,601-75,443,200 , GRCh37.p13 chr17: 73,437,682-73,439,281 TMEM94
    nsv6525501copy number variation1nstd223human GRCh38 chr17: 75,443,395-75,443,747 , GRCh37.p13 chr17: 73,439,476-73,439,828 TMEM94
    nsv6523812copy number variation1nstd223human GRCh38 chr17: 75,381,582-75,446,898 , GRCh37.p13 chr17: 73,377,663-73,442,979 MIR3678, GRB2, 2 more genes
    nsv6521888copy number variation1nstd223human GRCh38 chr17: 75,452,081-75,453,784 , GRCh37.p13 chr17: 73,448,162-73,449,865 TMEM94
    nsv6516801copy number variation1nstd223human GRCh38 chr17: 75,439,893-75,452,973 , GRCh37.p13 chr17: 73,435,974-73,449,054 TMEM94
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