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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7098188copy number variation1nstd102humanUncertain significance GRCh37 chr8: 94,798,431-94,935,901 , GRCh38.p12 chr8: 93,786,203-93,923,673 TMEM67, MIR378D2, 2 more genes
    nsv7098187copy number variation1nstd102humanPathogenic GRCh37 chr8: 94,770,691-94,777,894 , GRCh38.p12 chr8: 93,758,463-93,765,666 TMEM67
    nsv7098042copy number variation1nstd102humanPathogenic GRCh37 chr8: 94,767,143-94,935,901 , GRCh38.p12 chr8: 93,754,915-93,923,673 MYL12AP1, TMEM67, 2 more genes
    nsv7098041copy number variation1nstd102humanUncertain significance GRCh37 chr8: 94,767,143-94,828,680 , GRCh38.p12 chr8: 93,754,915-93,816,452 TMEM67
    nsv7097673copy number variation1nstd102humanPathogenic GRCh37 chr8: 94,821,048-94,821,409 , GRCh38.p12 chr8: 93,808,820-93,809,181 TMEM67
    nsv7097672copy number variation1nstd102humanPathogenic GRCh37 chr8: 94,808,184-94,818,223 , GRCh38.p12 chr8: 93,795,956-93,805,995 TMEM67
    nsv7077999inversion1nstd229human GRCh38 chr8: 90,977,597-95,722,625 , GRCh37.p13 chr8: 91,989,825-96,734,853 LINC02894, MIR3150B, 70 more genes
    nsv7066125inversion1nstd229human GRCh38 chr8: 93,806,459-93,812,990 , GRCh37.p13 chr8: 94,818,687-94,825,218 TMEM67
    nsv7060995inversion1nstd229human GRCh38 chr8: 93,804,951-93,809,450 , GRCh37.p13 chr8: 94,817,179-94,821,678 TMEM67
    nsv6852656copy number variation1nstd229human GRCh38 chr8: 93,809,901-94,281,700 , GRCh37.p13 chr8: 94,822,129-95,293,928 MYL12AP1, LOC105375648, 9 more genes
    nsv6845551copy number variation1nstd229human GRCh38 chr8: 93,791,801-93,794,500 , GRCh37.p13 chr8: 94,804,029-94,806,728 TMEM67
    nsv6843009copy number variation1nstd229human GRCh38 chr8: 93,825,515-93,827,974 , GRCh37.p13 chr8: 94,837,743-94,840,202 TMEM67
    nsv6841650copy number variation1nstd229human GRCh38 chr8: 93,797,086-93,804,759 , GRCh37.p13 chr8: 94,809,314-94,816,987 TMEM67
    nsv6839827copy number variation1nstd229human GRCh38 chr8: 93,697,601-93,814,700 , GRCh37.p13 chr8: 94,709,829-94,826,928 TMEM67, RBM12B, 4 more genes
    nsv6839229copy number variation1nstd229human GRCh38 chr8: 93,733,101-93,794,400 , GRCh37.p13 chr8: 94,745,329-94,806,628 RBM12B, RBM12B-DT, 2 more genes
    nsv6838883copy number variation1nstd229human GRCh38 chr8: 93,807,501-94,427,400 , GRCh37.p13 chr8: 94,819,729-95,439,628 LOC105375647, RPL6P23, 13 more genes
    nsv6838175copy number variation1nstd229human GRCh38 chr8: 93,785,245-93,796,414 , GRCh37.p13 chr8: 94,797,473-94,808,642 TMEM67
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
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