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Results: 1 to 20 of 925

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
nsv918292copy number variation1nstd75humanPathogenic NCBI36 (hg18) chr21: 13,322,592-46,921,373 , GRCh37 (hg19) chr21: 14,400,721-48,096,945 , GRCh38 chr21: 7,817,158-46,677,033 LINC00322, KRTAP25-1, 314 more genes
nsv918291copy number variation1nstd75humanBenign NCBI36 (hg18) chr15: 20,302,445-20,968,714 , GRCh37 (hg19) chr15: 22,751,081-23,417,273 , GRCh38 chr15: 22,455,823-23,121,987 TUBGCP5, NIPA1, 3 more genes
nsv918290copy number variation1nstd75humanBenign NCBI36 (hg18) chr14: 18,405,738-19,492,094 , GRCh37 (hg19) chr14: 19,335,738-20,422,254 , GRCh38 chr14: 18,559,261-19,954,095 OR4N2, OR4K2, 9 more genes
nsv918289copy number variation1nstd75humanBenign NCBI36 (hg18) chr10: 135,170,286-135,356,682 , GRCh37 (hg19) chr10: 135,320,296-135,506,692 , GRCh38 chr10: 133,506,792-133,769,367 CYP2E1, SPRNP1, 2 more genes
nsv918288copy number variation1nstd75humanBenign NCBI36 (hg18) chrY: 23,765,338-26,866,713 , GRCh37 (hg19) chrY: 25,355,950-28,457,325 , GRCh38 chrY: 23,209,803-26,311,178 LINC00266-4P, TTTY3, 13 more genes
nsv918287copy number variation1nstd75humanUncertain significance NCBI36 (hg18) chr22: 19,411,059-19,835,557 , GRCh37 (hg19) chr22: 21,081,059-21,505,557 , GRCh38 chr22: 20,726,771-21,151,268 CRKL, AIFM3, 9 more genes
nsv918286copy number variation1nstd75humanBenign NCBI36 (hg18) chr16: 34,339,342-34,634,885 , GRCh37 (hg19) chr16: 34,481,841-34,777,384 , GRCh38 chr16: 35,247,470-35,543,013 0
nsv918285copy number variation1nstd75humanBenign NCBI36 (hg18) chr15: 18,771,155-20,232,428 , GRCh37 (hg19) chr15: 20,511,141-22,681,064 , GRCh38 chr15: 20,305,888-22,308,242 POTEB2, MIR1268A, 11 more genes
nsv918284copy number variation1nstd75humanBenign NCBI36 (hg18) chrY: 23,925,462-25,390,960 , GRCh37 (hg19) chrY: 25,516,074-26,981,572 , GRCh38 chrY: 23,369,927-24,835,425 CDY1B, BPY2B, 6 more genes
nsv918282copy number variation1nstd75humanBenign NCBI36 (hg18) chr15: 18,845,989-19,889,588 , GRCh37 (hg19) chr15: 20,585,975-22,388,224 , GRCh38 chr15: 20,380,722-22,100,273 POTEB2, MIR3118-6, 8 more genes
nsv918281copy number variation1nstd75humanBenign NCBI36 (hg18) chr14: 106,102,068-106,250,892 , GRCh37 (hg19) chr14: 107,031,023-107,179,847 , GRCh37.p13 chr14|NW_004166863.1: 1,238,206-1,434,772 , GRCh38 chr14: 106,575,039-106,771,605 , GRCh38 chr14|NT_187600.1: 1,066,718-1,262,773 IGHV5-51, IGHV4-61, 8 more genes
nsv918280copy number variation1nstd75humanBenign NCBI36 (hg18) chr2: 88,917,230-89,374,858 , GRCh37 (hg19) chr2: 89,136,115-89,593,743 , GRCh38 chr2: 88,836,602-89,293,986 IGKV1-5, IGKV6-21, 25 more genes
nsv918279copy number variation1nstd75humanBenign NCBI36 (hg18) chr6: 224,113-236,734 , GRCh37 (hg19) chr6: 279,113-291,734 , GRCh38 chr6: 279,113-291,734 0
nsv918278copy number variation1nstd75humanBenign NCBI36 (hg18) chr6: 203,252-329,097 , GRCh37 (hg19) chr6: 258,252-384,097 , GRCh38 chr6: 258,252-384,097 DUSP22
nsv918277copy number variation2nstd75humanBenign NCBI36 (hg18) chr15: 19,103,563-20,232,428 , GRCh37 (hg19) chr15: 20,843,549-22,681,064 , GRCh38 chr15: 20,638,245-22,308,242 POTEB2, MIR1268A, 10 more genes
nsv918276copy number variation1nstd75humanLikely benign NCBI36 (hg18) chr8: 13,400,616-14,702,452 , GRCh37 (hg19) chr8: 13,356,245-14,658,081 , GRCh38 chr8: 13,498,736-14,800,572 RNA5SP255, DLC1, 2 more genes
nsv918275copy number variation1nstd75humanBenign NCBI36 (hg18) chr8: 7,256,028-8,168,239 , GRCh37 (hg19) chr8: 7,268,618-8,130,829 , GRCh38 chr8: 7,411,096-8,273,307 PRR23D1, FAM66E, 25 more genes
nsv918274copy number variation1nstd75humanBenign NCBI36 (hg18) chr10: 46,378,443-47,737,197 , GRCh37 (hg19) chr10: 46,958,437-48,117,191 , GRCh38 chr10: 46,157,935-47,923,579 FAM25BP, FAM25G, 20 more genes
nsv918273copy number variation1nstd75humanBenign NCBI36 (hg18) chr2: 89,632,330-91,328,405 , GRCh37 (hg19) chr2: 89,995,025-91,964,678 , GRCh38 chr2: 89,956,215-91,776,652 IGKV6D-41, IGKV6D-21, 14 more genes
nsv918272copy number variation1nstd75humanBenign NCBI36 (hg18) chr1: 146,797,047-148,142,443 , GRCh37 (hg19) chr1: 148,530,423-149,875,819 , GRCh38 chr1: 146,354,110-148,501,002 TRNAN-GUU, TRNAQ3, 59 more genes

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