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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
    nsv7056082inversion1nstd229human GRCh38 chr6: 34,111,345-34,120,541 , GRCh37.p13 chr6: 34,079,122-34,088,318 GRM4
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7050936inversion1nstd229human GRCh38 chr6: 34,122,404-34,122,483 , GRCh37.p13 chr6: 34,090,181-34,090,260 GRM4
    nsv7048348inversion1nstd229human GRCh38 chr6: 34,109,637-34,118,082 , GRCh37.p13 chr6: 34,077,414-34,085,859 GRM4
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv7040785inversion1nstd229human GRCh38 chr6: 34,050,417-34,053,416 , GRCh37.p13 chr6: 34,018,194-34,021,193 GRM4
    nsv7040770inversion1nstd229human GRCh38 chr6: 34,115,515-34,119,629 , GRCh37.p13 chr6: 34,083,292-34,087,406 GRM4
    nsv6797354copy number variation1nstd229human GRCh38 chr6: 34,026,801-34,031,300 , GRCh37.p13 chr6: 33,994,578-33,999,077 GRM4
    nsv6794920copy number variation1nstd229human GRCh38 chr6: 34,103,672-34,108,843 , GRCh37.p13 chr6: 34,071,449-34,076,620 GRM4
    nsv6794066copy number variation1nstd229human GRCh38 chr6: 34,075,041-34,075,096 , GRCh37.p13 chr6: 34,042,818-34,042,873 GRM4
    nsv6794065copy number variation1nstd229human GRCh38 chr6: 33,870,752-34,036,397 , GRCh37.p13 chr6: 33,838,529-34,004,174 LOC105375026, LOC107986590, 5 more genes
    nsv6792997copy number variation1nstd229human GRCh38 chr6: 34,064,600-34,069,228 , GRCh37.p13 chr6: 34,032,377-34,037,005 GRM4
    nsv6790092copy number variation1nstd229human GRCh38 chr6: 34,044,001-34,045,100 , GRCh37.p13 chr6: 34,011,778-34,012,877 GRM4
    nsv6787232copy number variation1nstd229human GRCh38 chr6: 34,034,869-34,034,927 , GRCh37.p13 chr6: 34,002,646-34,002,704 GRM4
    nsv6786862copy number variation1nstd229human GRCh38 chr6: 33,710,439-34,213,515 , GRCh37.p13 chr6: 33,678,216-34,181,292 GRM4, LOC105375024, 12 more genes
    nsv6783019copy number variation1nstd229human GRCh38 chr6: 34,155,433-34,157,596 , GRCh37.p13 chr6: 34,123,210-34,125,373 GRM4
    nsv6780917copy number variation1nstd229human GRCh38 chr6: 34,118,101-34,120,600 , GRCh37.p13 chr6: 34,085,878-34,088,377 GRM4
    nsv6779519copy number variation1nstd229human GRCh38 chr6: 34,071,872-34,073,265 , GRCh37.p13 chr6: 34,039,649-34,041,042 GRM4
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