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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2775876copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 127,658,004-135,427,143 , GRCh38 (hg38) chr10: 125,969,435-133,613,639 , NCBI36 (hg18) chr10: 127,647,994-135,277,133 ADGRA1-AS1, LINC01165, 59 more genes
    nsv2773480copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr4: 9,501,650-10,040,569 , GRCh38 (hg38) chr4: 9,500,006-10,038,945 , NCBI36 (hg18) chr4: 9,110,748-9,649,667 MIR548I2, RNA5SP154, 2 more genes
    nsv1067716copy number variation26nstd101humanBenign NCBI36 (hg18) chr2: 242,579,273-242,656,032 , GRCh37 (hg19) chr2: 242,930,600-243,007,359 , GRCh38 (hg38) chr2|NT_187523.1: 27,144-109,278 , GRCh38 (hg38) chr2: 241,988,449-242,065,208 , GRCh38 (hg38) chr2|NT_187647.1: 27,144-108,918 LINC01237, LINC01880
    nsv1067575copy number variation20nstd101humanBenign NCBI36 (hg18) chr10: 46,404,919-47,125,152 , GRCh37 (hg19) chr10: 47,006,954-47,531,169 , GRCh37.p13 chr10|NW_003871068.1: 431,049-2,010,264 , GRCh38 (hg38) chr10: 46,157,935-47,923,579 FAM25BP, FAM25G, 18 more genes
    nsv996156copy number variation1nstd37humanLikely benign GRCh37 (hg19) chr7: 24,143,492-24,671,708 , GRCh38 (hg38) chr7: 24,103,873-24,632,089 , NCBI36 (hg18) chr7: 24,110,017-24,638,233 RNA5SP228, NPY, 1 more genes
    nsv995284copy number variation2nstd37humanUncertain significance GRCh37 (hg19) chr9: 26,063,295-26,480,483 , GRCh38 (hg38) chr9: 26,063,297-26,480,485 , NCBI36 (hg18) chr9: 26,053,295-26,470,483 0
    nsv995235copy number variation10nstd37humanPathogenic, Likely pathogenic GRCh37 (hg19) chr7: 80,256,737-80,280,613 , GRCh38 (hg38) chr7: 80,627,421-80,651,297 , NCBI36 (hg18) chr7: 80,094,673-80,118,549 CD36
    nsv916999copy number variation3nstd37humanLikely benign NCBI36 (hg18) chr6: 32,071,800-32,116,990 , GRCh37 (hg19) chr6: 31,963,821-32,009,011 , GRCh37.p13 chr6|NT_167249.1: 3,296,531-3,341,719 , GRCh37.p13 chr6|NT_167247.1: 3,355,526-3,388,852 , GRCh38 (hg38) chr6: 31,996,044-32,041,234 , GRCh38 (hg38) chr6|NT_167247.2: 3,349,941-3,383,267 , GRCh38 (hg38) chr6|NT_167249.2: 3,297,233-3,342,421 C4B_2, CYP21A2, 3 more genes
    nsv916698copy number variation2nstd37humanLikely benign NCBI36 (hg18) chr14: 21,511,828-21,863,269 , GRCh37 (hg19) chr14: 22,441,988-22,793,429 , GRCh38 (hg38) chr14: 21,973,759-22,324,997 TRDV1, TRAV41, 25 more genes
    nsv869401copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr21: 34,801,570-34,987,550 , GRCh37 (hg19) chr21: 35,879,700-36,065,680 , GRCh38 (hg38) chr21: 34,507,402-34,693,381 RCAN1, KCNE1, 1 more genes
    nsv869400copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr2: 96,103,035-97,496,039 , GRCh37 (hg19) chr2: 96,739,308-98,108,185 , GRCh38 (hg38) chr2: 96,073,560-97,513,144 MIR3127, RNA5SP101, 25 more genes
    nsv533286copy number variation74nstd37humanBenign, Likely benign NCBI36 (hg18) chr16: 34,339,573-34,584,866 , GRCh37 (hg19) chr16: 34,482,072-34,727,365 , GRCh38 (hg38) chr16: 35,247,701-35,492,994 RARRES2P6, LINC01566
    nsv532531copy number variation1nstd101humanUncertain significance NCBI36 (hg18) chr16: 30,278,051-30,489,321 , GRCh37 (hg19) chr16: 30,370,550-30,581,820 , GRCh38 (hg38) chr16: 30,359,229-30,570,499 MIR4518, ZNF688, 11 more genes
    nsv530875copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr6: 109,633-5,768,833 , GRCh37 (hg19) chr6: 164,633-5,823,834 , GRCh38 (hg38) chr6: 164,633-5,823,601 HMGN2P28, LYRM4-AS1, 46 more genes
    nsv530796copy number variation1nstd101humanUncertain significance NCBI36 (hg18) chr14: 75,025,148-75,504,061 , GRCh37 (hg19) chr14: 75,955,395-76,434,308 , GRCh38 (hg38) chr14: 75,489,052-75,967,965 MIR7641-2, BATF, 4 more genes
    nsv530263copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr3: 195,626,514-199,380,026 , GRCh37 (hg19) chr3: 194,145,225-197,895,629 , GRCh38 (hg38) chr3: 194,424,496-198,168,758 MIR922, FRG2FP, 62 more genes
    nsv529218copy number variation71nstd37humanBenign NCBI36 (hg18) chr10: 135,104,029-135,227,522 , GRCh37 (hg19) chr10: 135,254,039-135,377,532 , GRCh38 (hg38) chr10: 133,440,535-133,564,028 CYP2E1, SYCE1
    nsv529216copy number variation153nstd37humanBenign NCBI36 (hg18) chr6: 204,528-238,493 , GRCh37 (hg19) chr6: 259,528-293,493 , GRCh38 (hg38) chr6: 259,528-293,493 DUSP22
    nsv497803copy number variation45nstd37humanBenign, Likely benign NCBI36 (hg18) chr5: 69,274,445-70,622,775 , GRCh37 (hg19) chr5: 69,238,689-70,587,019 , GRCh38 (hg38) chr5: 69,942,862-71,291,192 GUSBP9, GTF2H2, 6 more genes
    nsv497787copy number variation102nstd37humanBenign NCBI36 (hg18) chr8: 7,156,920-7,843,637 , GRCh37 (hg19) chr8: 7,169,510-7,806,227 , GRCh38 (hg38) chr8: 7,311,988-7,948,705 FAM66B, PRR23D1, 25 more genes
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