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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv6993359copy number variation1nstd229human GRCh38 chr16: 67,531,184-67,534,232 , GRCh37.p13 chr16: 67,565,087-67,568,135 RIPOR1
    nsv6992862copy number variation1nstd229human GRCh38 chr16: 67,372,949-67,543,806 , GRCh37.p13 chr16: 67,406,852-67,577,709 AGRP, RNU1-123P, 8 more genes
    nsv6992582copy number variation1nstd229human GRCh38 chr16: 67,514,001-67,519,800 , GRCh37.p13 chr16: 67,547,904-67,553,703 LOC100505942, RIPOR1
    nsv6990211copy number variation1nstd229human GRCh38 chr16: 67,518,778-67,520,892 , GRCh37.p13 chr16: 67,552,681-67,554,795 LOC100505942, RIPOR1
    nsv6985230copy number variation1nstd229human GRCh38 chr16: 67,514,518-67,521,541 , GRCh37.p13 chr16: 67,548,421-67,555,444 LOC100505942, RIPOR1
    nsv6981265copy number variation1nstd229human GRCh38 chr16: 67,524,352-67,527,536 , GRCh37.p13 chr16: 67,558,255-67,561,439 LOC100505942, RIPOR1
    nsv6979646copy number variation1nstd229human GRCh38 chr16: 67,530,430-67,545,678 , GRCh37.p13 chr16: 67,564,333-67,579,581 RIPOR1
    nsv6978720copy number variation1nstd229human GRCh38 chr16: 67,514,090-67,527,163 , GRCh37.p13 chr16: 67,547,993-67,561,066 LOC100505942, RIPOR1
    nsv6978615copy number variation1nstd229human GRCh38 chr16: 67,522,001-67,528,136 , GRCh37.p13 chr16: 67,555,904-67,562,039 RIPOR1, LOC100505942
    nsv6501687copy number variation1nstd223human GRCh38 chr16: 67,514,089-67,527,162 , GRCh37.p13 chr16: 67,547,992-67,561,065 RIPOR1, LOC100505942
    nsv6495798copy number variation1nstd223human GRCh38 chr16: 67,518,801-67,520,900 , GRCh37.p13 chr16: 67,552,704-67,554,803 LOC100505942, RIPOR1
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6189742copy number variation1nstd214human GRCh38 chr16: 67,522,137-67,522,311 , GRCh37.p13 chr16: 67,556,040-67,556,214 LOC100505942, RIPOR1
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv5704253mobile element insertion1nstd211human GRCh38 chr16: 67,531,830-67,531,830 , GRCh37.p13 chr16: 67,565,733-67,565,733 RIPOR1
    nsv5530615copy number variation1nstd206human GRCh38 chr16: 67,531,181-67,534,242 , GRCh37.p13 chr16: 67,565,084-67,568,145 RIPOR1
    nsv5521826copy number variation1nstd206human GRCh38 chr16: 67,519,912-67,523,408 , GRCh37.p13 chr16: 67,553,815-67,557,311 LOC100505942, RIPOR1
    nsv5429825mobile element insertion1nstd206human GRCh38 chr16: 67,531,830-67,531,881 , GRCh37.p13 chr16: 67,565,733-67,565,784 RIPOR1
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