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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713457mobile element insertion1nstd211human GRCh38 chr8: 60,938,493-60,938,493 , GRCh37.p13 chr8: 61,851,052-61,851,052 NASPP1
    nsv5696154mobile element insertion1nstd211human GRCh38 chr8: 60,940,336-60,940,336 , GRCh37.p13 chr8: 61,852,895-61,852,895 NASPP1
    nsv5410107mobile element insertion1nstd206human GRCh38 chr8: 60,940,336-60,940,357 , GRCh37.p13 chr8: 61,852,895-61,852,916 NASPP1
    nsv5401940mobile element insertion1nstd206human GRCh38 chr8: 60,938,493-60,938,544 , GRCh37.p13 chr8: 61,851,052-61,851,103 NASPP1
    nsv4965377copy number variation1nstd200human GRCh38 chr8: 60,828,994-60,963,415 , GRCh37.p13 chr8: 61,741,553-61,875,974 NASPP1, LOC105375938, 3 more genes
    nsv4716589copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 60,026,663-63,779,735 , GRCh38.p12 chr8: 59,114,104-62,867,176 ASPH, CA8, 36 more genes
    nsv4498207mobile element insertion1nstd166human GRCh37.p13 chr8: 61,851,038-61,851,038 , GRCh38.p12 chr8: 60,938,479-60,938,479 NASPP1
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3959457copy number variation1nstd168human GRCh38 chr8: 60,936,555-60,965,521 , GRCh37.p13 chr8: 61,849,114-61,878,080 CLVS1, NASPP1, 1 more genes
    nsv3924415copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,431,781-67,571,260 , GRCh38 chr8: 60,519,222-66,659,025 , NCBI36 chr8: 61,594,335-67,733,814 RN7SKP135, TRIM55, 77 more genes
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 NUDT15P1, LINC01301, 83 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923110copy number variation1nstd102humanPathogenic GRCh37 chr8: 57,838,371-62,604,418 , NCBI36 chr8: 58,000,925-62,766,972 , GRCh38 chr8: 56,925,812-61,691,859 LOC105375855, LOC105375858, 50 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 more genes
    nsv3916768copy number variation1nstd102humanPathogenic NCBI36 chr8: 47,062,121-70,378,576 , GRCh37 chr8: 46,942,956-70,216,022 , GRCh38 chr8: 46,031,334-69,303,787 RPL7L1P18, LINC03018, 316 more genes
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