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Items: 1 to 20 of 15302

  • The following term was not found in dbVar: ill.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3170336copy number variation1nstd45humanPathogenic GRCh38.p12 chr2: 182,924,851-183,038,858 , GRCh37 chr2: 183,789,579-183,903,586 NCKAP1
    nsv508690copy number variation4nstd49human NCBI35 chr1: 204,066,136-204,158,829 , GRCh38.p12 chr1: 207,504,396-207,597,089 , GRCh37.p13 chr1: 207,677,741-207,770,434 CR1
    nsv508333copy number variation4nstd49human GRCh38.p12 chr4: 172,448,535-172,526,524 , GRCh37.p13 chr4: 173,369,686-173,447,675 , NCBI35 chr4: 173,744,416-173,822,405 GALNTL6
    nsv508384copy number variation4nstd49human NCBI35 chr5: 151,418,775-151,467,519 , GRCh37.p13 chr5: 151,438,582-151,487,326 , GRCh38.p12 chr5: 152,059,021-152,107,765 LINC01933
    nsv508672copy number variation3nstd49human NCBI35 chr12: 44,170,997-44,217,358 , GRCh38.p12 chr12: 45,490,947-45,537,308 , GRCh37.p13 chr12: 45,884,730-45,931,091 LOC105369743
    nsv510577copy number variation3nstd49human NCBI35 chr13: 29,111,612-29,152,316 , GRCh38.p12 chr13: 29,639,475-29,680,179 , GRCh37.p13 chr13: 30,213,612-30,254,316 LOC102723345
    nsv508649copy number variation4nstd49human NCBI35 chr11: 92,780,547-92,820,740 , GRCh37.p13 chr11: 93,140,899-93,181,092 , GRCh38.p12 chr11: 93,407,733-93,447,926 DEUP1
    nsv508358copy number variation4nstd49human NCBI35 chr5: 57,708,987-57,745,441 , GRCh37.p13 chr5: 57,673,230-57,709,684 , GRCh38.p12 chr5: 58,377,403-58,413,857 LOC105378984
    nsv508655copy number variation3nstd49human NCBI35 chr11: 106,727,851-106,762,695 , GRCh37.p13 chr11: 107,222,641-107,257,485 , GRCh38.p12 chr11: 107,351,915-107,386,759 CWF19L2
    nsv508529copy number variation2nstd49human GRCh38.p12 chr8: 131,257,065-131,291,015 , NCBI35 chr8: 132,338,494-132,372,444 , GRCh37.p13 chr8: 132,269,312-132,303,262 LOC105375760
    nsv508666copy number variation3nstd49human NCBI35 chr12: 13,418,770-13,451,305 , GRCh38.p12 chr12: 13,374,569-13,407,104 , GRCh37.p13 chr12: 13,527,503-13,560,038 LINC01559
    nsv508267copy number variation4nstd49human GRCh37.p13 chr3: 192,856,362-192,887,886 , GRCh38.p12 chr3: 193,138,573-193,170,097 , NCBI35 chr3: 194,339,064-194,370,588 VEZF1P1
    nsv508527copy number variation4nstd49human GRCh38.p12 chr8: 128,446,324-128,472,555 , NCBI35 chr8: 129,527,752-129,553,983 , GRCh37.p13 chr8: 129,458,570-129,484,801 LINC00824
    nsv510585copy number variation4nstd49human NCBI35 chr13: 49,955,885-49,981,784 , GRCh38.p12 chr13: 50,483,748-50,509,647 , GRCh37.p13 chr13: 51,057,884-51,083,783 DLEU1
    nsv510870copy number variation3nstd49human NCBI35 chrX: 154,479,739-154,503,773 , GRCh37.p13 chrX: 154,916,035-154,940,069 , GRCh38.p12 chrX: 155,686,374-155,710,408 SPRY3
    nsv510845copy number variation4nstd49human NCBI35 chrX: 85,393,874-85,417,323 , GRCh37.p13 chrX: 85,587,729-85,611,178 , GRCh38.p12 chrX: 86,332,726-86,356,175 DACH2
    nsv508714copy number variation4nstd49human GRCh38.p12 chr2: 19,014,015-19,035,998 , NCBI35 chr2: 19,121,454-19,157,380 , GRCh37.p13 chr2: 19,199,826-19,235,752 LINC01376
    nsv508329copy number variation3nstd49human GRCh38.p12 chr4: 166,753,309-166,772,583 , GRCh37.p13 chr4: 167,674,460-167,693,734 , NCBI35 chr4: 168,049,190-168,068,464 SPOCK3
    nsv508290copy number variation4nstd49human GRCh38.p12 chr4: 78,337,998-78,356,821 , GRCh37.p13 chr4: 79,259,152-79,277,975 , NCBI35 chr4: 79,616,331-79,635,154 FRAS1
    nsv508292copy number variation3nstd49human GRCh38.p12 chr4: 79,962,413-79,981,161 , GRCh37.p13 chr4: 80,883,567-80,902,315 , NCBI35 chr4: 81,240,746-81,259,494 ANTXR2
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