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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980132inversion1nstd209human GRCh38 chr12: 21,873,888-24,109,273 , GRCh37.p13 chr12: 22,026,822-24,262,207 , ST8SIA1, 19 more genes
    nsv5977074insertion1nstd209human GRCh38 chr12: 21,933,009-21,933,009 , GRCh37.p13 chr12: 22,085,943-22,085,943 ABCC9
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5920337copy number variation1nstd209human GRCh38 chr12: 21,928,337-21,928,453 , GRCh37.p13 chr12: 22,081,271-22,081,387 ABCC9
    nsv5919215copy number variation1nstd209human GRCh38 chr12: 21,912,032-21,912,124 , GRCh37.p13 chr12: 22,064,966-22,065,058 ABCC9
    nsv5919148copy number variation1nstd209human GRCh38 chr12: 21,894,539-21,894,640 , GRCh37.p13 chr12: 22,047,473-22,047,574 ABCC9
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5861783copy number variation1nstd209human GRCh38 chr12: 21,826,106-21,828,481 , GRCh37.p13 chr12: 21,979,040-21,981,415 ABCC9, LOC105369689
    nsv5853079copy number variation1nstd209human GRCh38 chr12: 21,908,316-21,910,315 , GRCh37.p13 chr12: 22,061,250-22,063,249 ABCC9
    nsv5727031mobile element insertion1nstd211human GRCh38 chr12: 21,930,457-21,930,457 , GRCh37.p13 chr12: 22,083,391-22,083,391 ABCC9
    nsv5720384mobile element insertion1nstd211human GRCh38 chr12: 21,886,084-21,886,084 , GRCh37.p13 chr12: 22,039,018-22,039,018 ABCC9
    nsv5702761mobile element insertion2nstd211human GRCh38 chr12: 21,863,784-21,863,784 , GRCh37.p13 chr12: 22,016,718-22,016,718 ABCC9
    nsv5699583mobile element insertion1nstd211human GRCh38 chr12: 21,867,978-21,867,978 , GRCh37.p13 chr12: 22,020,912-22,020,912 ABCC9
    nsv5695105mobile element insertion2nstd211human GRCh38 chr12: 21,933,021-21,933,021 , GRCh37.p13 chr12: 22,085,955-22,085,955 ABCC9
    nsv5660157insertion1nstd207human GRCh38 chr12: 21,933,009-21,933,009 , GRCh37.p13 chr12: 22,085,943-22,085,943 ABCC9
    nsv5599760copy number variation1nstd207human GRCh38 chr12: 21,928,337-21,928,453 , GRCh37.p13 chr12: 22,081,271-22,081,387 ABCC9
    nsv5598231copy number variation1nstd207human GRCh38 chr12: 21,894,539-21,894,640 , GRCh37.p13 chr12: 22,047,473-22,047,574 ABCC9
    nsv5564133copy number variation1nstd102humanUncertain significance GRCh37 chr12: 22,089,457-22,089,618 , GRCh38.p12 chr12: 21,936,523-21,936,684 ABCC9
    nsv5551639insertion1nstd206human GRCh38 chr12: 21,809,733-21,809,737 , GRCh37.p13 chr12: 21,962,667-21,962,671 ABCC9, LOC105369689
    nsv5549192insertion1nstd206human GRCh38 chr12: 21,933,009-21,933,009 , GRCh37.p13 chr12: 22,085,943-22,085,943 ABCC9
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