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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6855547copy number variation1nstd229human GRCh38 chr8: 37,859,141-37,859,199 , GRCh37.p13 chr8: 37,716,659-37,716,717 RAB11FIP1
    nsv6850277copy number variation1nstd229human GRCh38 chr8: 37,819,401-37,869,600 , GRCh37.p13 chr8: 37,676,919-37,727,118 RAB11FIP1, ADGRA2, 1 more genes
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6569389inversion1nstd223human GRCh38 chr8: 37,877,739-37,878,488 , GRCh37.p13 chr8: 37,735,257-37,736,006 RAB11FIP1
    nsv6565273inversion1nstd223human GRCh38 chr8: 37,857,027-37,857,634 , GRCh37.p13 chr8: 37,714,545-37,715,152 RAB11FIP1
    nsv6429577copy number variation1nstd223human GRCh38 chr8: 37,888,119-37,890,076 , GRCh37.p13 chr8: 37,745,637-37,747,594 RAB11FIP1
    nsv6426987copy number variation1nstd223human GRCh38 chr8: 37,880,501-37,889,992 , GRCh37.p13 chr8: 37,738,019-37,747,510 RAB11FIP1
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv6291079copy number variation1nstd102humanUncertain significance GRCh37 chr8: 37,544,476-37,818,465 , GRCh38.p12 chr8: 37,686,958-37,960,947 ZNF703, BRF2, 10 more genes
    nsv6137281copy number variation1nstd213human GRCh37 chr8: 37,350,000-38,410,001 , GRCh38.p12 chr8: 37,492,482-38,552,483 ADRB3, EIF4EBP1, 32 more genes
    nsv6136672copy number variation1nstd213human GRCh37 chr8: 37,710,000-37,880,001 , GRCh38.p12 chr8: 37,852,482-38,022,483 ADRB3, RAB11FIP1, 2 more genes
    nsv5926636copy number variation1nstd209human GRCh38 chr8: 37,859,141-37,859,196 , GRCh37.p13 chr8: 37,716,659-37,716,714 RAB11FIP1
    nsv5926448copy number variation1nstd209human GRCh38 chr8: 37,886,154-37,887,161 , GRCh37.p13 chr8: 37,743,672-37,744,679 RAB11FIP1
    nsv5639211insertion1nstd207human GRCh38 chr8: 37,894,725-37,894,725 , GRCh37.p13 chr8: 37,752,243-37,752,243 RAB11FIP1
    nsv5630079insertion1nstd207human GRCh38 chr8: 37,863,252-37,863,252 , GRCh37.p13 chr8: 37,720,770-37,720,770 RAB11FIP1
    nsv5540654insertion1nstd206human GRCh38 chr8: 37,867,477-37,867,477 , GRCh37.p13 chr8: 37,724,995-37,724,995 RAB11FIP1
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