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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713944mobile element insertion2nstd211human GRCh38 chr8: 24,492,475-24,492,475 , GRCh37.p13 chr8: 24,349,988-24,349,988 ADAM7, ADAM7-AS1, 1 more genes
    nsv5699189mobile element insertion2nstd211human GRCh38 chr8: 24,494,476-24,494,476 , GRCh37.p13 chr8: 24,351,989-24,351,989 ADAM7, ADAM7-AS1, 1 more genes
    nsv5493237copy number variation1nstd206human GRCh38 chr8: 24,503,107-24,503,209 , GRCh37.p13 chr8: 24,360,620-24,360,722 ADAM7-AS1, ADAM7, 1 more genes
    nsv5485756copy number variation1nstd206human GRCh38 chr8: 24,506,515-24,506,597 , GRCh37.p13 chr8: 24,364,028-24,364,110 ADAM7-AS1, ADAM7, 1 more genes
    nsv5413047mobile element insertion1nstd206human GRCh38 chr8: 24,494,476-24,494,527 , GRCh37.p13 chr8: 24,351,989-24,352,040 ADAM7, ADAM7-AS1, 1 more genes
    nsv5396905mobile element insertion1nstd206human GRCh38 chr8: 24,492,475-24,492,526 , GRCh37.p13 chr8: 24,349,988-24,350,039 ADAM7, ADAM7-AS1, 1 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5188980mobile element insertion1nstd203human GRCh38 chr8: 24,507,560-24,507,576 , GRCh37.p13 chr8: 24,365,073-24,365,089 ADAM7, ADAM7-AS1, 1 more genes
    nsv5119562mobile element insertion1nstd203human GRCh38 chr8: 24,494,464-24,494,476 , GRCh37.p13 chr8: 24,351,977-24,351,989 ADAM7, ADAM7-AS1, 1 more genes
    nsv5112844mobile element insertion1nstd203human GRCh38 chr8: 24,492,460-24,492,475 , GRCh37.p13 chr8: 24,349,973-24,349,988 ADAM7, ADAM7-AS1, 1 more genes
    nsv5105491mobile element insertion1nstd203human GRCh38 chr8: 24,492,467-24,492,472 , GRCh37.p13 chr8: 24,349,980-24,349,985 ADAM7, ADAM7-AS1, 1 more genes
    nsv5102362mobile element insertion1nstd203human GRCh38 chr8: 24,492,459-24,492,475 , GRCh37.p13 chr8: 24,349,972-24,349,988 ADAM7, ADAM7-AS1, 1 more genes
    nsv5029529inversion1nstd200human GRCh38 chr8: 23,965,527-24,582,482 , GRCh37.p13 chr8: 23,823,040-24,439,995 ADAM7, ADAM28, 7 more genes
    nsv4959728copy number variation1nstd200human GRCh38 chr8: 24,435,386-24,511,059 , GRCh37.p13 chr8: 24,292,899-24,368,572 ADAM7, ADAM7-AS1, 1 more genes
    nsv4821514copy number variation1nstd200human GRCh37 chr8: 24,292,899-24,368,572 , GRCh38.p12 chr8: 24,435,386-24,511,059 ADAM7-AS1, ADAM7, 1 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4712461copy number variation1nstd195human GRCh37 chr8: 24,312,101-24,417,001 , GRCh38.p12 chr8: 24,454,588-24,559,488 ADAM7, ADAM7-AS1, 2 more genes
    nsv4679597copy number variation1nstd189human GRCh37.p13 chr8: 23,970,950-24,353,039 , GRCh38.p12 chr8: 24,113,437-24,495,526 ADAM7, ADAM28, 4 more genes
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