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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957601insertion1nstd209human GRCh38 chr1: 115,304,329-115,304,329 , GRCh37.p13 chr1: 115,846,950-115,846,950 NGF-AS1, NGF
    nsv5694180mobile element insertion2nstd211human GRCh38 chr1: 115,303,098-115,303,098 , GRCh37.p13 chr1: 115,845,719-115,845,719 NGF, NGF-AS1
    nsv5690922mobile element insertion1nstd211human GRCh38 chr1: 115,321,874-115,321,874 , GRCh37.p13 chr1: 115,864,495-115,864,495 NGF, NGF-AS1
    nsv5417828copy number variation1nstd206human GRCh38 chr1: 115,181,665-115,561,209 , GRCh37.p13 chr1: 115,724,286-116,103,830 , LOC112268234, 3 more genes
    nsv5415221copy number variation1nstd206human GRCh38 chr1: 115,318,319-115,318,459 , GRCh37.p13 chr1: 115,860,940-115,861,080 NGF, NGF-AS1
    nsv5411291mobile element insertion1nstd206human GRCh38 chr1: 115,303,098-115,303,149 , GRCh37.p13 chr1: 115,845,719-115,845,770 NGF-AS1, NGF
    nsv5397100mobile element insertion1nstd206human GRCh38 chr1: 115,321,874-115,321,915 , GRCh37.p13 chr1: 115,864,495-115,864,536 NGF-AS1, NGF
    nsv5381204copy number variation1nstd102humanUncertain significance GRCh37 chr1: 115,828,681-115,829,426 , GRCh38.p12 chr1: 115,286,060-115,286,805 NGF-AS1, NGF
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5200969copy number variation1nstd204human GRCh38.p13 chr1: 115,324,401-115,337,200 , GRCh37.p13 chr1: 115,867,022-115,879,821 NGF-AS1, NGF
    nsv5079756mobile element insertion1nstd203human GRCh38 chr1: 115,303,074-115,303,098 , GRCh37.p13 chr1: 115,845,695-115,845,719 NGF-AS1, NGF
    nsv5077231mobile element insertion1nstd203human GRCh38 chr1: 115,304,329-115,304,345 , GRCh37.p13 chr1: 115,846,950-115,846,966 NGF-AS1, NGF
    nsv5069666mobile element insertion1nstd203human GRCh38 chr1: 115,303,081-115,303,098 , GRCh37.p13 chr1: 115,845,702-115,845,719 NGF, NGF-AS1
    nsv5067459mobile element insertion1nstd203human GRCh38 chr1: 115,321,860-115,321,871 , GRCh37.p13 chr1: 115,864,481-115,864,492 NGF, NGF-AS1
    nsv5063731mobile element insertion1nstd203human GRCh38 chr1: 115,337,247-115,337,247 , GRCh37.p13 chr1: 115,879,868-115,879,868 NGF-AS1, NGF
    nsv4890911copy number variation1nstd200human GRCh38 chr1: 115,306,412-115,306,623 , GRCh37.p13 chr1: 115,849,033-115,849,244 NGF, NGF-AS1
    nsv4781141copy number variation1nstd200human GRCh37 chr1: 115,724,285-116,103,831 , GRCh38.p12 chr1: 115,181,664-115,561,210 , ELOCP20, 3 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
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