MyVariants table
You can view MyVariants when you open the Analyses tab, then click MyVariants. The MyVariants table includes specific information such as genome location and mutation type. The following columns of information are available in the MyVariants table.
Information type |
Description |
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MyVariants flag options:
This column can be edited. |
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Information that researchers add to the MyVariants in note format. This column can be edited. |
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The location of the variant on a specific chromosome. This column can be sorted. |
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Classifications that can be set for MyVariants. For more information, see Apply flags, notes, or classifications to variants of interest. This column can be edited. |
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The gene or genes where the variant is found. This column can be sorted. |
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The genotype sequence (ATCG). This column can be sorted. |
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The reference sequence. This column can be sorted. |
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The type of variant or call, such as SNV, CNV, Fusion, or REF. This column can be sorted. |
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The name of analysis where the variant was identified. |
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The name of sample where the variant was identified. |
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The observed allele variation. This column can be sorted. |
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The copy number variation. This column can be sorted. |
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The copy number subtype. This column can be sorted. |
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The identifier of the variant. This column can be sorted. |