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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138920insertion1nstd232human GRCh37.p13 chr6: 149,900,111-149,900,111 , GRCh38.p12 chr6: 149,578,975-149,578,975 GINM1
    nsv7050873inversion1nstd229human GRCh38 chr6: 149,562,064-149,571,470 , GRCh37.p13 chr6: 149,883,200-149,892,606 GINM1
    nsv6817688copy number variation1nstd229human GRCh38 chr6: 149,564,889-149,584,183 , GRCh37.p13 chr6: 149,886,025-149,905,319 GINM1
    nsv6809336copy number variation1nstd229human GRCh38 chr6: 149,584,901-149,590,100 , GRCh37.p13 chr6: 149,906,037-149,911,236 GINM1
    nsv6806931copy number variation1nstd229human GRCh38 chr6: 149,574,168-149,574,304 , GRCh37.p13 chr6: 149,895,304-149,895,440 GINM1
    nsv6799087copy number variation1nstd229human GRCh38 chr6: 149,557,486-149,572,503 , GRCh37.p13 chr6: 149,878,622-149,893,639 GINM1
    nsv6631089copy number variation1nstd224human GRCh37 chr6: 149,893,443-149,903,597 , GRCh38.p12 chr6: 149,572,307-149,582,461 GINM1
    nsv6618674copy number variation1nstd223human GRCh38 chr6: 149,571,172-149,571,958 , GRCh37.p13 chr6: 149,892,308-149,893,094 GINM1
    nsv6617755copy number variation1nstd223human GRCh38 chr6: 149,564,897-149,584,139 , GRCh37.p13 chr6: 149,886,033-149,905,275 GINM1
    nsv6606501copy number variation1nstd223human GRCh38 chr6: 149,573,266-149,573,590 , GRCh37.p13 chr6: 149,894,402-149,894,726 GINM1
    nsv6571422inversion1nstd223human GRCh38 chr6: 146,996,555-151,115,323 , GRCh37.p13 chr6: 147,317,691-151,436,459 RPSAP40, STXBP5, 62 more genes
    nsv6567447inversion1nstd223human GRCh38 chr6: 149,572,675-149,573,292 , GRCh37.p13 chr6: 149,893,811-149,894,428 GINM1
    nsv6564529inversion1nstd223human GRCh38 chr6: 149,579,711-149,581,459 , GRCh37.p13 chr6: 149,900,847-149,902,595 GINM1
    nsv6560583inversion1nstd223human GRCh38 chr6: 149,562,060-149,571,472 , GRCh37.p13 chr6: 149,883,196-149,892,608 GINM1
    nsv6305495copy number variation1nstd186human GRCh37 chr6: 149,892,236-149,894,181 , GRCh38.p12 chr6: 149,571,100-149,573,045 GINM1
    nsv6140631copy number variation1nstd206human GRCh38 chr6: 149,564,790-149,571,000 , GRCh37.p13 chr6: 149,885,926-149,892,136 GINM1
    nsv6064915insertion1nstd212human GRCh38 chr6: 149,574,185-149,574,185 , GRCh37.p13 chr6: 149,895,321-149,895,321 GINM1
    nsv6000921copy number variation1nstd212human GRCh38 chr6: 149,591,033-149,592,374 , GRCh37.p13 chr6: 149,912,169-149,913,510 RPS18P9, GINM1
    nsv5895313copy number variation1nstd209human GRCh38 chr6: 149,574,168-149,574,303 , GRCh37.p13 chr6: 149,895,304-149,895,439 GINM1
    nsv5639215insertion1nstd207human GRCh38 chr6: 149,574,168-149,574,168 , GRCh37.p13 chr6: 149,895,304-149,895,304 GINM1
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