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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3157402copy number variation1nstd151human GRCh37 (hg19) chr17: 18,387,186-21,826,303 , GRCh38 (hg38) chr17: 18,483,872-22,299,697 ALDH3A1, FOXO3B, 135 more genes
    nsv3154661copy number variation2nstd151human GRCh37 (hg19) chr17: 20,798,987-20,906,391 , GRCh38 (hg38) chr17: 20,895,674-21,003,078 USP22, LOC339260, 4 more genes
    nsv3153973copy number variation1nstd151human GRCh37 (hg19) chr17: 20,768,725-20,911,314 , GRCh38 (hg38) chr17: 20,865,412-21,008,001 USP22, RNASEH1P1, 5 more genes
    nsv3152964copy number variation1nstd151human GRCh37 (hg19) chr17: 19,609,958-21,319,961 , GRCh38 (hg38) chr17: 19,706,645-21,416,649 KCNJ12, MAP2K3, 59 more genes
    nsv3152530copy number variation1nstd151human GRCh37 (hg19) chr17: 20,356,327-20,906,391 , GRCh38 (hg38) chr17: 20,453,014-21,003,078 CDRT15L2, RNASEH1P1, 30 more genes
    nsv3151984copy number variation1nstd151human GRCh37 (hg19) chr17: 20,361,493-20,906,391 , GRCh38 (hg38) chr17: 20,458,180-21,003,078 CCDC144NL, KRT17P7, 30 more genes
    nsv3149713copy number variation1nstd151human GRCh37 (hg19) chr17: 20,768,725-20,931,992 , GRCh38 (hg38) chr17: 20,865,412-21,028,679 CCDC144NL, CCDC144NL-AS1, 5 more genes
    nsv3146373copy number variation2nstd151human GRCh37 (hg19) chr17: 20,798,987-20,908,308 , GRCh38 (hg38) chr17: 20,895,674-21,004,995 LOC105369205, USP22, 4 more genes
    nsv3144951copy number variation1nstd151human GRCh37 (hg19) chr17: 20,798,987-21,102,158 , GRCh38 (hg38) chr17: 20,895,674-21,198,845 TMEM11, USP22, 7 more genes
    nsv3143809copy number variation1nstd151human GRCh37 (hg19) chr17: 20,796,702-20,908,308 , GRCh38 (hg38) chr17: 20,893,389-21,004,995 USP22, LOC339260, 5 more genes
    nsv3138863copy number variation2nstd151human GRCh37 (hg19) chr17: 20,768,725-21,826,303 , GRCh38 (hg38) chr17: 20,865,412-22,299,697 CCDC144NL, CCDC144NL-AS1, 30 more genes
    nsv3138661copy number variation2nstd151human GRCh37 (hg19) chr17: 20,363,662-20,906,391 , GRCh38 (hg38) chr17: 20,460,349-21,003,078 CDRT15L2, KRT17P6, 30 more genes
    nsv3136860copy number variation1nstd151human GRCh37 (hg19) chr2: 3,196,182-3,624,271 , GRCh38 (hg38) chr2: 3,192,411-3,576,681 RNASEH1, LOC112268321, 5 more genes
    nsv3134398copy number variation1nstd151human GRCh37 (hg19) chr2: 41,605-3,774,672 , GRCh38 (hg38) chr2: 41,605-3,727,082 RNASEH1, TPO, 48 more genes
    nsv3131708copy number variation1nstd151human GRCh37 (hg19) chr2: 3,597,960-3,605,855 , GRCh38 (hg38) chr2: 3,550,370-3,558,265 RNASEH1, RNASEH1-AS1
    nsv3127845copy number variation1nstd151human GRCh37 (hg19) chr2: 3,481,461-3,652,065 , GRCh38 (hg38) chr2: 3,477,690-3,604,475 RNASEH1, TRAPPC12, 5 more genes
    nsv3127721copy number variation1nstd151human GRCh37 (hg19) chr2: 3,196,182-3,774,672 , GRCh38 (hg38) chr2: 3,192,411-3,727,082 RNASEH1, EIPR1, 11 more genes
    nsv3122614copy number variation1nstd151human GRCh37 (hg19) chr2: 3,358,318-3,750,156 , GRCh38 (hg38) chr2: 3,354,547-3,702,566 RNASEH1, EIPR1, 11 more genes
    nsv3119531copy number variation1nstd151human GRCh37 (hg19) chr2: 1,795,009-3,774,672 , GRCh38 (hg38) chr2: 1,791,237-3,727,082 RNASEH1, TRAPPC12, 20 more genes
    nsv3119294copy number variation1nstd151human GRCh37 (hg19) chr2: 3,447,496-3,692,237 , GRCh38 (hg38) chr2: 3,443,725-3,644,647 RNASEH1, COLEC11, 7 more genes
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