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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5212241copy number variation1nstd204human GRCh38.p13 chr1: 28,084,401-28,971,400 , GRCh37.p13 chr1: 28,410,912-29,297,912 SNORA73B, ARL8BP2, 29 more genes
    nsv4903268copy number variation1nstd200human GRCh38 chr1: 28,238,359-28,239,852 , GRCh37.p13 chr1: 28,564,870-28,566,363 ATP5IF1
    nsv4903267copy number variation1nstd200human GRCh38 chr1: 28,233,771-28,235,222 , GRCh37.p13 chr1: 28,560,282-28,561,733 ATP5IF1
    nsv4903266copy number variation1nstd200human GRCh38 chr1: 28,221,047-28,245,306 , GRCh37.p13 chr1: 28,547,558-28,571,817 ATP5IF1, DNAJC8
    nsv4895594copy number variation1nstd200human GRCh38 chr1: 28,234,335-28,235,410 , GRCh37.p13 chr1: 28,560,846-28,561,921 ATP5IF1
    nsv4780732copy number variation1nstd200human GRCh37 chr1: 28,564,870-28,566,363 , GRCh38.p12 chr1|NW_018654706.1: 32,003-33,496 , GRCh38.p12 chr1: 28,238,359-28,239,852 ATP5IF1
    nsv4780731copy number variation1nstd200human GRCh37 chr1: 28,560,282-28,561,733 , GRCh38.p12 chr1: 28,233,771-28,235,222 , GRCh38.p12 chr1|NW_018654706.1: 27,415-28,866 ATP5IF1
    nsv4780730copy number variation1nstd200human GRCh37 chr1: 28,552,373-28,564,551 , GRCh38.p12 chr1|NW_018654706.1: 19,506-31,684 , GRCh38.p12 chr1: 28,225,862-28,238,040 DNAJC8, ATP5IF1
    nsv4772804copy number variation1nstd200human GRCh37 chr1: 28,560,846-28,561,921 , GRCh38.p12 chr1: 28,234,335-28,235,410 , GRCh38.p12 chr1|NW_018654706.1: 27,979-29,054 ATP5IF1
    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
    nsv4594454copy number variation1nstd183human GRCh37 chr1: 28,284,815-28,955,102 , GRCh38.p12 chr1: 27,958,304-28,628,590 RNU6ATAC27P, ARL8BP2, 26 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4048097copy number variation1nstd166human GRCh37.p13 chr1: 28,562,483-28,562,544 , GRCh38.p12 chr1|NW_018654706.1: 29,616-29,677 , GRCh38.p12 chr1: 28,235,972-28,236,033 ATP5IF1
    nsv4037918copy number variation1nstd166human GRCh37.p13 chr1: 28,564,688-28,564,781 , GRCh38.p12 chr1|NW_018654706.1: 31,821-31,914 , GRCh38.p12 chr1: 28,238,177-28,238,270 ATP5IF1
    nsv3967935copy number variation1nstd168human GRCh38 chr1: 28,216,301-28,300,395 , GRCh37.p13 chr1: 28,542,812-28,626,906 ATP5IF1, DNAJC8, 1 more genes
    nsv3907483copy number variation1nstd102humanPathogenic GRCh37 chr1: 27,289,536-32,744,646 , GRCh38 chr1: 26,963,045-32,279,045 , NCBI36 chr1: 27,162,123-32,517,233 ATP5IF1, LOC102723760, 138 more genes
    nsv3901163copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937 TMEM222, ZBTB8OS, 453 more genes
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