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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv6978050copy number variation1nstd229human GRCh38 chr16: 4,063,701-4,088,200 , GRCh37.p13 chr16: 4,113,702-4,138,201 ADCY9
    nsv6977331copy number variation1nstd229human GRCh38 chr16: 3,963,001-3,966,700 , GRCh37.p13 chr16: 4,013,002-4,016,701 ADCY9
    nsv6977215copy number variation1nstd229human GRCh38 chr16: 4,083,201-4,091,200 , GRCh37.p13 chr16: 4,133,202-4,141,201 ADCY9
    nsv6977028copy number variation1nstd229human GRCh38 chr16: 4,025,200-4,120,399 , GRCh37.p13 chr16: 4,075,201-4,170,400 ADCY9
    nsv6976878copy number variation1nstd229human GRCh38 chr16: 3,948,069-3,951,507 , GRCh37.p13 chr16: 3,998,070-4,001,508 LINC02861, ADCY9
    nsv6976357copy number variation1nstd229human GRCh38 chr16: 3,959,741-3,962,196 , GRCh37.p13 chr16: 4,009,742-4,012,197 ADCY9
    nsv6972191copy number variation1nstd229human GRCh38 chr16: 4,106,343-4,106,389 , GRCh37.p13 chr16: 4,156,344-4,156,390 ADCY9
    nsv6972032copy number variation1nstd229human GRCh38 chr16: 3,960,290-3,961,188 , GRCh37.p13 chr16: 4,010,291-4,011,189 ADCY9
    nsv6971591copy number variation1nstd229human GRCh38 chr16: 4,011,564-4,022,223 , GRCh37.p13 chr16: 4,061,565-4,072,224 ADCY9
    nsv6971195copy number variation1nstd229human GRCh38 chr16: 4,084,346-4,091,059 , GRCh37.p13 chr16: 4,134,347-4,141,060 ADCY9
    nsv6970795copy number variation1nstd229human GRCh38 chr16: 3,987,966-3,988,017 , GRCh37.p13 chr16: 4,037,967-4,038,018 ADCY9
    nsv6970793copy number variation1nstd229human GRCh38 chr16: 3,981,695-4,165,587 , GRCh37.p13 chr16: 4,031,696-4,215,588 ADCY9, DBIP3
    nsv6970760copy number variation1nstd229human GRCh38 chr16: 4,084,213-4,091,176 , GRCh37.p13 chr16: 4,134,214-4,141,177 ADCY9
    nsv6970342copy number variation1nstd229human GRCh38 chr16: 4,086,237-4,095,406 , GRCh37.p13 chr16: 4,136,238-4,145,407 ADCY9
    nsv6970180copy number variation1nstd229human GRCh38 chr16: 4,079,468-4,082,156 , GRCh37.p13 chr16: 4,129,469-4,132,157 ADCY9
    nsv6970162copy number variation1nstd229human GRCh38 chr16: 4,085,182-4,095,894 , GRCh37.p13 chr16: 4,135,183-4,145,895 ADCY9
    nsv6969793copy number variation1nstd229human GRCh38 chr16: 4,026,601-4,035,300 , GRCh37.p13 chr16: 4,076,602-4,085,301 ADCY9
    nsv6968703copy number variation1nstd229human GRCh38 chr16: 3,997,902-4,005,462 , GRCh37.p13 chr16: 4,047,903-4,055,463 ADCY9
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