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  • The following terms were not found in dbVar: 168054702, XP_001779769.1.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3879671copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,524,176-55,604,729 , GRCh38.p12 chr4: 54,658,009-54,738,563 KIT
    nsv3876106copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,284,190-161,332,229 , GRCh38 chr1: 161,314,400-161,362,439 SDHC
    nsv4683629copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 17,345,376-17,380,514 , GRCh38.p12 chr1: 17,018,881-17,054,019 SDHB
    nsv6310921copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,349,093-17,380,514 , GRCh38.p12 chr1: 17,022,598-17,054,019 SDHB
    nsv5673240copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,376-17,371,403 , GRCh38.p12 chr1: 17,018,881-17,044,908 SDHB
    nsv4682910copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,366-17,371,393 , GRCh38.p12 chr1: 17,018,871-17,044,898 SDHB
    nsv4683305copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 17,345,376-17,371,393 , GRCh38.p12 chr1: 17,018,881-17,044,898 SDHB
    nsv4682055copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 161,310,374-161,332,308 , GRCh38.p12 chr1: 161,340,584-161,362,518 SDHC
    nsv7095713copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,359,545-17,380,514 , GRCh38.p12 chr1: 17,033,050-17,054,019 SDHB
    nsv4682124copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,310,374-161,326,640 , GRCh38.p12 chr1: 161,340,584-161,356,850 SDHC
    nsv6314872copy number variation1nstd102humanPathogenic GRCh38 chr1: 17,048,756-17,064,430 , GRCh37.p13 chr1: 17,375,251-17,390,925 SDHB
    nsv4683776copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,366-17,359,650 , GRCh38.p12 chr1: 17,018,871-17,033,155 SDHB
    nsv3873146copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,370-17,359,646 , GRCh38 chr1: 17,018,875-17,033,151 SDHB
    nsv6310920copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,345,376-17,359,650 , GRCh38.p12 chr1: 17,018,881-17,033,155 SDHB
    nsv4681738copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,371,246-17,380,514 , GRCh38.p12 chr1: 17,044,751-17,054,019 SDHB
    nsv4682694copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 161,326,457-161,332,308 , GRCh38.p12 chr1: 161,356,667-161,362,518 SDHC
    nsv3889669copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,326,457-161,332,233 , GRCh38 chr1: 161,356,667-161,362,443 SDHC
    nsv4681917copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,293,394-161,298,297 , GRCh38.p12 chr1: 161,323,604-161,328,507 SDHC
    nsv5381063copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 161,332,109-161,332,308 , GRCh38.p12 chr1: 161,362,319-161,362,518 SDHC
    nsv7097257copy number variation1nstd102humanPathogenic GRCh37 chr4: 55,569,880-55,570,068 , GRCh38.p12 chr4: 54,703,714-54,703,902 KIT
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