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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 CUTA, SYNGAP1, 184 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7055128inversion1nstd229human GRCh38 chr6: 36,461,671-36,465,545 , GRCh37.p13 chr6: 36,429,448-36,433,322 KCTD20
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7050356inversion1nstd229human GRCh38 chr6: 36,449,365-36,616,701 , GRCh37.p13 chr6: 36,417,142-36,584,478 RN7SL748P, STK38, 3 more genes
    nsv7050048inversion1nstd229human GRCh38 chr6: 36,457,520-36,614,610 , GRCh37.p13 chr6: 36,425,297-36,582,387 SRSF3, STK38, 2 more genes
    nsv7048540inversion1nstd229human GRCh38 chr6: 36,461,676-36,462,211 , GRCh37.p13 chr6: 36,429,453-36,429,988 KCTD20
    nsv7046729inversion1nstd229human GRCh38 chr6: 35,747,390-37,934,033 , GRCh37.p13 chr6: 35,715,167-37,901,809 MAPK14, LAP3P2, 58 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6797598copy number variation1nstd229human GRCh38 chr6: 36,191,801-36,462,400 , GRCh37.p13 chr6: 36,159,578-36,430,177 RN7SL502P, BRPF3, 8 more genes
    nsv6797128copy number variation1nstd229human GRCh38 chr6: 36,481,528-36,481,718 , GRCh37.p13 chr6: 36,449,305-36,449,495 KCTD20
    nsv6792523copy number variation1nstd229human GRCh38 chr6: 36,484,371-36,487,041 , GRCh37.p13 chr6: 36,452,148-36,454,818 KCTD20
    nsv6792187copy number variation1nstd229human GRCh38 chr6: 36,465,001-36,492,500 , GRCh37.p13 chr6: 36,432,778-36,460,277 STK38, KCTD20
    nsv6790699copy number variation1nstd229human GRCh38 chr6: 36,468,359-36,472,632 , GRCh37.p13 chr6: 36,436,136-36,440,409 KCTD20
    nsv6789403copy number variation1nstd229human GRCh38 chr6: 36,480,501-36,480,542 , GRCh37.p13 chr6: 36,448,278-36,448,319 KCTD20
    nsv6788534copy number variation1nstd229human GRCh38 chr6: 36,459,075-36,477,876 , GRCh37.p13 chr6: 36,426,852-36,445,653 KCTD20
    nsv6785492copy number variation1nstd229human GRCh38 chr6: 36,450,573-36,454,389 , GRCh37.p13 chr6: 36,418,350-36,422,166 KCTD20, RN7SL502P
    nsv6784794copy number variation1nstd229human GRCh38 chr6: 36,449,301-36,457,500 , GRCh37.p13 chr6: 36,417,078-36,425,277 KCTD20, RN7SL502P
    nsv6784202copy number variation1nstd229human GRCh38 chr6: 36,490,638-36,674,466 , GRCh37.p13 chr6: 36,458,415-36,642,243 SRSF3, STK38, 8 more genes
    nsv6783868copy number variation1nstd229human GRCh38 chr6: 36,462,835-36,467,456 , GRCh37.p13 chr6: 36,430,612-36,435,233 KCTD20
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