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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127699insertion1nstd186human GRCh37 chr10: 71,169,645-71,169,676 , GRCh38.p12 chr10: 69,409,889-69,409,920 TACR2
    nsv5588930copy number variation1nstd207human GRCh38 chr10: 69,409,865-69,409,914 , GRCh37.p13 chr10: 71,169,621-71,169,670 TACR2
    nsv5585998copy number variation1nstd207human GRCh38 chr10: 69,408,814-69,408,867 , GRCh37.p13 chr10: 71,168,570-71,168,623 TACR2
    nsv5535999insertion1nstd206human GRCh38 chr10: 69,409,889-69,409,920 , GRCh37.p13 chr10: 71,169,645-71,169,676 TACR2
    nsv5481040copy number variation1nstd206human GRCh38 chr10: 69,401,213-69,402,175 , GRCh37.p13 chr10: 71,160,969-71,161,931 HK1, TACR2
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976386copy number variation1nstd200human GRCh38 chr10: 69,416,273-69,416,914 , GRCh37.p13 chr10: 71,176,029-71,176,670 TACR2
    nsv4973748copy number variation1nstd200human GRCh38 chr10: 69,398,954-69,416,462 , GRCh37.p13 chr10: 71,158,710-71,176,218 HK1, TACR2
    nsv4841421copy number variation1nstd200human GRCh37 chr10: 71,176,030-71,176,670 , GRCh38.p12 chr10: 69,416,274-69,416,914 TACR2
    nsv4835641copy number variation1nstd200human GRCh37 chr10: 71,158,710-71,176,218 , GRCh38.p12 chr10: 69,398,954-69,416,462 HK1, TACR2
    nsv4740363copy number variation1nstd199human GRCh37 chr10: 71,168,539-71,168,608 , GRCh38.p12 chr10: 69,408,783-69,408,852 TACR2
    nsv4737830copy number variation1nstd199human GRCh37 chr10: 71,169,611-71,169,665 , GRCh38.p12 chr10: 69,409,855-69,409,909 TACR2
    nsv4601421copy number variation1nstd183human GRCh37 chr10: 70,564,120-74,122,461 , GRCh38.p12 chr10: 68,804,363-72,362,703 , SGPL1, 79 more genes
    nsv4438405copy number variation1nstd175human GRCh37 chr10: 71,169,621-71,169,673 , GRCh38.p12 chr10: 69,409,865-69,409,917 TACR2
    nsv4368564copy number variation1nstd173human GRCh37 chr10: 71,118,183-71,195,499 , GRCh38.p12 chr10: 69,358,427-69,435,743 TACR2, HK1, 1 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3950757copy number variation1nstd167human GRCh37 chr10: 71,169,621-71,169,672 , GRCh38.p12 chr10: 69,409,865-69,409,916 TACR2
    nsv3938281copy number variation1nstd167human GRCh37 chr10: 71,169,623-71,169,675 , GRCh38.p12 chr10: 69,409,867-69,409,919 TACR2
    nsv3925413copy number variation1nstd167human GRCh37 chr10: 71,168,620-71,168,653 , GRCh38.p12 chr10: 69,408,864-69,408,897 TACR2
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