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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5418140copy number variation1nstd206human GRCh38 chr1: 153,072,587-153,094,587 , GRCh37.p13 chr1: 153,045,063-153,067,063 SPRR2E
    nsv5417997copy number variation1nstd206human GRCh38 chr1: 153,070,587-153,093,400 , GRCh37.p13 chr1: 153,043,063-153,065,876 SPRR2E, SPRR2B
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5282019copy number variation1nstd204human GRCh38.p13 chr1: 153,085,423-153,104,391 , GRCh37.p13 chr1: 153,057,899-153,076,867 SPRR2E
    nsv5281260copy number variation1nstd204human GRCh37.p13 chr1: 153,021,569-153,075,143 , GRCh38.p13 chr1: 153,049,093-153,102,667 SPRR2A, SPRR2B, 1 more genes
    nsv5211848copy number variation1nstd204human GRCh38.p13 chr1: 153,085,439-153,104,382 , GRCh37.p13 chr1: 153,057,915-153,076,858 SPRR2E
    nsv4897433copy number variation1nstd200human GRCh38 chr1: 153,094,939-153,099,161 , GRCh37.p13 chr1: 153,067,415-153,071,637 SPRR2E
    nsv4897432copy number variation1nstd200human GRCh38 chr1: 153,092,982-153,111,903 , GRCh37.p13 chr1: 153,065,458-153,084,379 SPRR2F, SPRR2E
    nsv4897431copy number variation1nstd200human GRCh38 chr1: 153,090,469-153,096,436 , GRCh37.p13 chr1: 153,062,945-153,068,912 SPRR2E
    nsv4774030copy number variation1nstd200human GRCh37 chr1: 153,067,415-153,071,637 , GRCh38.p12 chr1: 153,094,939-153,099,161 SPRR2E
    nsv4774029copy number variation1nstd200human GRCh37 chr1: 153,062,945-153,068,912 , GRCh38.p12 chr1: 153,090,469-153,096,436 SPRR2E
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4728602copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,007,105-153,463,223 , GRCh38.p12 chr1: 153,034,629-153,490,747 S100A8, S100A7P1, 23 more genes
    nsv4715955copy number variation1nstd195human GRCh37 chr1: 153,052,551-153,080,351 , GRCh38.p12 chr1: 153,080,075-153,107,875 SPRR2E
    nsv4673972copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,061,323-153,904,594 , GRCh38.p12 chr1: 153,088,847-153,932,118 S100A15A, LOC343052, 46 more genes
    nsv4518402copy number variation1nstd166human GRCh37.p13 chr1: 152,648,171-153,289,950 , GRCh38.p12 chr1: 152,675,695-153,317,474 SPRR2D, SMCP, 36 more genes
    nsv4402521copy number variation1nstd174human GRCh37 chr1: 153,042,430-153,069,958 , GRCh38.p12 chr1: 153,069,954-153,097,482 SPRR2B, SPRR2E
    nsv4394163copy number variation1nstd174human GRCh37 chr1: 153,043,113-153,067,949 , GRCh38.p12 chr1: 153,070,637-153,095,473 SPRR2E, SPRR2B
    nsv4061733copy number variation1nstd166human GRCh37.p13 chr1: 153,065,553-153,182,302 , GRCh38.p12 chr1: 153,093,077-153,209,826 SPRR2C, SPRR2E, 4 more genes
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