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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146883copy number variation1nstd232human GRCh37.p13 chr19: 59,060,276-59,060,352 , GRCh38.p12 chr19: 58,548,909-58,548,985 TRIM28, MIR6807
    nsv7145593copy number variation1nstd232human GRCh37.p13 chr19: 59,060,605-59,060,694 , GRCh38.p12 chr19: 58,549,238-58,549,327 TRIM28, MIR6807
    nsv7145438copy number variation1nstd232human GRCh38.p12 chr19: 58,549,649-58,549,734 , GRCh37.p13 chr19: 59,061,016-59,061,101 TRIM28, CHMP2A, 1 more genes
    nsv7143895copy number variation1nstd232human GRCh38.p12 chr19: 58,549,859-58,549,946 , GRCh37.p13 chr19: 59,061,226-59,061,313 TRIM28, CHMP2A, 1 more genes
    nsv7143257copy number variation1nstd232human GRCh37.p13 chr19: 59,058,878-59,058,962 , GRCh38.p12 chr19: 58,547,511-58,547,595 TRIM28
    nsv7142285copy number variation1nstd232human GRCh38.p12 chr19: 58,550,282-58,550,373 , GRCh37.p13 chr19: 59,061,649-59,061,740 TRIM28, CHMP2A, 1 more genes
    nsv7141011insertion1nstd232human GRCh37.p13 chr19: 59,056,463-59,056,463 , GRCh38.p12 chr19: 58,545,096-58,545,096 TRIM28
    nsv7138310copy number variation1nstd232human GRCh37.p13 chr19: 59,059,774-59,059,850 , GRCh38.p12 chr19: 58,548,407-58,548,483 TRIM28, MIR6807
    nsv7138160copy number variation1nstd232human GRCh37.p13 chr19: 59,059,080-59,059,157 , GRCh38.p12 chr19: 58,547,713-58,547,790 TRIM28
    nsv7004413copy number variation1nstd229human GRCh38 chr19: 58,482,045-58,546,365 , GRCh37.p13 chr19: 58,993,412-59,057,732 RN7SL525P, TRIM28, 7 more genes
    nsv6625057copy number variation1nstd224human GRCh37 chr19: 59,059,921-59,082,361 , GRCh38.p12 chr19: 58,548,554-58,570,994 MZF1, UBE2M, 4 more genes
    nsv6146576copy number variation1nstd206human GRCh38 chr19: 58,504,874-58,592,874 , GRCh37.p13 chr19: 59,016,241-59,104,241 , RN7SL525P, 11 more genes
    nsv6133477copy number variation1nstd213human GRCh37 chr19: 57,800,000-59,128,983 , GRCh38.p12 chr19: 57,288,632-58,607,616 A1BG, FKBP1AP1, 95 more genes
    nsv6133413copy number variation1nstd213human GRCh37 chr19: 57,870,000-59,128,983 , GRCh38.p12 chr19: 57,358,632-58,607,616 ZNF8, ZNF211, 92 more genes
    nsv6109678insertion1nstd212human GRCh38 chr19: 58,542,389-58,542,389 , GRCh37.p13 chr19: 59,053,756-59,053,756 TRIM28, ZBTB45, 1 more genes
    nsv6104021insertion1nstd212human GRCh38 chr19: 58,542,142-58,542,142 , GRCh37.p13 chr19: 59,053,509-59,053,509 TRIM28, ZBTB45, 1 more genes
    nsv6055596copy number variation1nstd212human GRCh38 chr19: 58,539,414-58,542,126 , GRCh37.p13 chr19: 59,050,781-59,053,493 TRIM28, ZBTB45, 1 more genes
    nsv6053623copy number variation1nstd212human GRCh38 chr19: 58,543,226-58,543,355 , GRCh37.p13 chr19: 59,054,593-59,054,722 RN7SL525P, TRIM28
    nsv6052086copy number variation1nstd212human GRCh38 chr19: 58,542,158-58,542,357 , GRCh37.p13 chr19: 59,053,525-59,053,724 TRIM28, ZBTB45, 1 more genes
    nsv5885343copy number variation2nstd209human GRCh38 chr19: 58,543,058-58,544,789 , GRCh37.p13 chr19: 59,054,425-59,056,156 ZBTB45, RN7SL525P, 1 more genes
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