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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7098849copy number variation1nstd102humanPathogenic GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065 ATG3, SIDT1, 81 more genes
    nsv7051524inversion1nstd229human GRCh38 chr3: 110,492,556-118,654,181 , GRCh37.p13 chr3: 110,211,403-118,373,028 MIR8076, ZBTB20-AS4, 106 more genes
    nsv7046343inversion1nstd229human GRCh38 chr3: 108,261,187-113,011,016 , GRCh37.p13 chr3: 107,980,034-112,729,863 LOC105374041, DIMT1P1, 69 more genes
    nsv7042841inversion1nstd229human GRCh38 chr3: 104,903,601-112,515,639 , GRCh37.p13 chr3: 104,622,445-112,234,486 MTND4P16, CD47, 94 more genes
    nsv7039416inversion1nstd229human GRCh38 chr3: 111,765,090-113,399,244 , GRCh37.p13 chr3: 111,483,937-113,118,091 SLC9C1, TAGLN3, 35 more genes
    nsv6701576copy number variation1nstd229human GRCh38 chr3: 109,882,767-113,954,905 , GRCh37.p13 chr3: 109,601,614-113,673,752 SLC9C1, NECTIN3, 64 more genes
    nsv6636830copy number variation1nstd102humanPathogenic GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409 ATP6V1A, DRD3, 117 more genes
    nsv6628254copy number variation1nstd224human GRCh37 chr3: 106,647,916-112,127,787 , GRCh38.p12 chr3: 106,929,069-112,408,940 CD47, CD96, 71 more genes
    nsv6315408copy number variation1nstd102humanPathogenic GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849 DZIP3, MIR9900, 138 more genes
    nsv6280424insertion1nstd214human GRCh38 chr3: 112,005,863-112,005,863 , GRCh37.p13 chr3: 111,724,710-111,724,710 TAGLN3
    nsv6149266copy number variation1nstd214human GRCh38 chr3: 112,005,865-112,005,921 , GRCh37.p13 chr3: 111,724,712-111,724,768 TAGLN3
    nsv6134776copy number variation1nstd213human GRCh37 chr3: 105,120,000-116,510,001 , GRCh38.p12 chr3: 105,401,156-116,791,154 , ALCAM, 156 more genes
    nsv5991440copy number variation1nstd212human GRCh38 chr3: 112,005,873-112,005,936 , GRCh37.p13 chr3: 111,724,720-111,724,783 TAGLN3
    nsv5889235copy number variation1nstd209human GRCh38 chr3: 112,005,865-112,005,921 , GRCh37.p13 chr3: 111,724,712-111,724,768 TAGLN3
    nsv5555923sequence alteration1nstd206human GRCh38 chr3: 111,599,044-112,091,945 , GRCh37.p13 chr3: 111,317,891-111,810,792 ABHD10, PLCXD2, 10 more genes
    nsv5302598copy number variation1nstd204human GRCh38.p13 chr3: 109,643,426-112,176,826 , GRCh37.p13 chr3: 109,362,273-111,895,673 , NECTIN3-AS1, 28 more genes
    nsv5229675copy number variation1nstd204human GRCh38.p13 chr3: 111,834,401-112,176,600 , GRCh37.p13 chr3: 111,553,248-111,895,447 TMPRSS7, PLCXD2, 10 more genes
    nsv5227908copy number variation1nstd204human GRCh38.p13 chr3: 112,012,206-112,014,210 , GRCh37.p13 chr3: 111,731,053-111,733,057 TAGLN3
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
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