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Results: 1 to 20 of 81345

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv616030copy number variation1nstd54human NCBI36 (hg18) chr9: 140,191,939-140,208,462 , GRCh37 (hg19) chr9: 141,072,118-141,088,641 , GRCh38 (hg38) chr9: 138,177,666-138,198,191 0
    nsv616029copy number variation2nstd54human NCBI36 (hg18) chr9: 140,191,763-140,208,462 , GRCh37 (hg19) chr9: 141,071,942-141,088,641 , GRCh38 (hg38) chr9: 138,177,490-138,198,191 0
    nsv616028copy number variation1nstd54human NCBI36 (hg18) chr9: 140,146,139-140,225,046 , GRCh37 (hg19) chr9: 141,026,318-141,105,225 , GRCh38 (hg38) chr9: 138,131,866-138,214,775 0
    nsv616027copy number variation1nstd54human NCBI36 (hg18) chr9: 140,124,766-140,147,760 , GRCh37 (hg19) chr9: 141,004,945-141,027,939 , GRCh38 (hg38) chr9: 138,110,493-138,133,487 CACNA1B
    nsv616026copy number variation1nstd54human NCBI36 (hg18) chr9: 140,111,180-140,137,173 , GRCh37 (hg19) chr9: 140,991,359-141,017,352 , GRCh38 (hg38) chr9: 138,096,907-138,122,900 CACNA1B
    nsv616025copy number variation1nstd54human NCBI36 (hg18) chr9: 139,986,010-140,147,760 , GRCh37 (hg19) chr9: 140,866,189-141,027,939 , GRCh38 (hg38) chr9: 137,971,737-138,133,487 CACNA1B
    nsv616024copy number variation1nstd54human NCBI36 (hg18) chr9: 139,534,231-139,655,919 , GRCh37 (hg19) chr9: 140,414,410-140,536,098 , GRCh38 (hg38) chr9: 137,519,958-137,641,646 ZMYND19, PNPLA7, 5 more genes
    nsv616023copy number variation1nstd54human NCBI36 (hg18) chr9: 139,492,391-139,722,708 , GRCh37 (hg19) chr9: 140,372,570-140,602,887 , GRCh38 (hg38) chr9: 137,478,118-137,708,435 ZMYND19, PNPLA7, 5 more genes
    nsv616022copy number variation1nstd54human NCBI36 (hg18) chr9: 139,492,391-139,643,250 , GRCh37 (hg19) chr9: 140,372,570-140,523,429 , GRCh38 (hg38) chr9: 137,478,118-137,628,977 ZMYND19, PNPLA7, 5 more genes
    nsv616021copy number variation1nstd54human NCBI36 (hg18) chr9: 139,448,962-139,467,094 , GRCh37 (hg19) chr9: 140,329,141-140,347,273 , GRCh38 (hg38) chr9: 137,434,689-137,452,821 MIR7114, NSMF, 1 more genes
    nsv616020copy number variation1nstd54human NCBI36 (hg18) chr9: 139,243,405-139,353,200 , GRCh37 (hg19) chr9: 140,123,584-140,233,379 , GRCh38 (hg38) chr9: 137,229,132-137,338,927 C9orf173-AS1, TUBB4B, 7 more genes
    nsv616019copy number variation1nstd54human NCBI36 (hg18) chr9: 139,238,269-139,338,799 , GRCh37 (hg19) chr9: 140,118,448-140,218,978 , GRCh38 (hg38) chr9: 137,223,996-137,324,526 C9orf173-AS1, TUBB4B, 8 more genes
    nsv616018copy number variation1nstd54human NCBI36 (hg18) chr9: 139,238,269-139,332,463 , GRCh37 (hg19) chr9: 140,118,448-140,212,642 , GRCh38 (hg38) chr9: 137,223,996-137,318,190 C9orf173-AS1, TUBB4B, 8 more genes
    nsv616017copy number variation1nstd54human NCBI36 (hg18) chr9: 139,214,426-139,342,132 , GRCh37 (hg19) chr9: 140,094,605-140,222,311 , GRCh38 (hg38) chr9: 137,200,153-137,327,859 C9orf173-AS1, TUBB4B, 12 more genes
    nsv616016copy number variation1nstd54human NCBI36 (hg18) chr9: 139,214,426-139,332,463 , GRCh37 (hg19) chr9: 140,094,605-140,212,642 , GRCh38 (hg38) chr9: 137,200,153-137,318,190 C9orf173-AS1, TUBB4B, 12 more genes
    nsv616015copy number variation1nstd54human NCBI36 (hg18) chr9: 139,214,426-139,320,576 , GRCh37 (hg19) chr9: 140,094,605-140,200,755 , GRCh38 (hg38) chr9: 137,200,153-137,306,303 C9orf173-AS1, TUBB4B, 11 more genes
    nsv616014copy number variation1nstd54human NCBI36 (hg18) chr9: 139,212,255-139,247,686 , GRCh37 (hg19) chr9: 140,092,434-140,127,865 , GRCh38 (hg38) chr9: 137,197,982-137,233,413 SLC34A3, NDOR1, 4 more genes
    nsv616013copy number variation2nstd54human NCBI36 (hg18) chr9: 139,211,953-139,247,686 , GRCh37 (hg19) chr9: 140,092,132-140,127,865 , GRCh38 (hg38) chr9: 137,197,680-137,233,413 SLC34A3, NDOR1, 4 more genes
    nsv616012copy number variation1nstd54human NCBI36 (hg18) chr9: 139,211,953-139,238,107 , GRCh37 (hg19) chr9: 140,092,132-140,118,286 , GRCh38 (hg38) chr9: 137,197,680-137,223,834 NDOR1, TPRN, 2 more genes
    nsv616011copy number variation1nstd54human NCBI36 (hg18) chr9: 139,205,812-139,244,013 , GRCh37 (hg19) chr9: 140,085,991-140,124,192 , GRCh38 (hg38) chr9: 137,191,539-137,229,740 NDOR1, TPRN, 3 more genes

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