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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045293inversion1nstd229human GRCh38 chr5: 73,247,847-76,069,477 , GRCh37.p13 chr5: 72,543,674-75,365,302 LOC107986423, NSA2, 48 more genes
    nsv6773834copy number variation1nstd229human GRCh38 chr5: 73,583,654-73,583,719 , GRCh37.p13 chr5: 72,879,479-72,879,544 UTP15
    nsv6764931copy number variation1nstd229human GRCh38 chr5: 73,578,868-73,578,937 , GRCh37.p13 chr5: 72,874,693-72,874,762 UTP15
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6565718inversion1nstd223human GRCh38 chr5: 73,573,754-73,574,202 , GRCh37.p13 chr5: 72,869,579-72,870,027 UTP15
    nsv6308311insertion1nstd186human GRCh37 chr5: 72,874,762-72,874,762 , GRCh38.p12 chr5: 73,578,937-73,578,937 UTP15
    nsv6285018insertion1nstd214human GRCh38 chr5: 73,578,891-73,578,891 , GRCh37.p13 chr5: 72,874,716-72,874,716 UTP15
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv5966469insertion1nstd209human GRCh38 chr5: 73,578,888-73,578,888 , GRCh37.p13 chr5: 72,874,713-72,874,713 UTP15
    nsv5549950insertion1nstd206human GRCh38 chr5: 73,578,937-73,578,937 , GRCh37.p13 chr5: 72,874,762-72,874,762 UTP15
    nsv5462771copy number variation1nstd206human GRCh38 chr5: 73,581,531-73,590,130 , GRCh37.p13 chr5: 72,877,356-72,885,955 UTP15
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4675088copy number variation1nstd102humanUncertain significance GRCh37 chr5: 72,829,994-74,076,751 , GRCh38.p12 chr5: 73,534,169-74,780,926 NSA2, RNU7-196P, 17 more genes
    nsv4593253copy number variation1nstd183human GRCh37 chr5: 72,874,772-72,875,783 , GRCh38.p12 chr5: 73,578,947-73,579,958 UTP15
    nsv4542487insertion1nstd166human GRCh37.p13 chr5: 72,874,721-72,874,721 , GRCh38.p12 chr5: 73,578,896-73,578,896 UTP15
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
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