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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4729459copy number variation1nstd102humanLikely benign GRCh37 chr7: 76,696,035-76,849,523 , GRCh38.p12 chr7: 77,066,718-77,220,206 FGL2, CCDC146, 4 more genes
    nsv4675627copy number variation1nstd102humanUncertain significance GRCh37 chr7: 76,784,372-77,199,666 , GRCh38.p12 chr7: 77,155,055-77,570,349 GCNT1P5, PTPN12, 6 more genes
    nsv4613459copy number variation1nstd183human GRCh37 chr7: 76,823,328-76,828,328 , GRCh38.p12 chr7: 77,194,011-77,199,011 FGL2, CCDC146
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3961828copy number variation1nstd168human GRCh38 chr7: 77,170,276-77,203,584 , GRCh37.p13 chr7: 76,799,593-76,832,901 FGL2, CCDC146
    nsv3922762copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112 PMS2P3, RCC1L, 142 more genes
    nsv3921264copy number variation1nstd102humanPathogenic NCBI36 chr7: 74,963,960-77,842,828 , GRCh37 chr7: 75,126,024-78,004,892 , GRCh38 chr7: 75,496,701-78,375,575 PMS2P11, CCDC146, 56 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3919663copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 71,282,013-78,631,323 , GRCh37 chr7: 71,644,077-78,793,387 , GRCh38 chr7: 72,179,092-79,164,071 CLDN4, CLDN3, 149 more genes
    nsv3918722copy number variation1nstd102humanPathogenic GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909 GTF2IP1, POM121, 184 more genes
    nsv3917211copy number variation1nstd102humanPathogenic GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058 HSPB1, UFC1P1, 123 more genes
    nsv3913861copy number variation1nstd102humanBenign NCBI36 chr7: 75,983,981-76,661,373 , GRCh37.p13 chr7: 76,146,045-76,823,437 , GRCh38.p12 chr7: 76,516,728-77,194,120 PMS2P11, LOC100422695, 16 more genes
    nsv3913396copy number variation1nstd102humanUncertain significance GRCh37 chr7: 76,069,874-77,809,560 , NCBI36 chr7: 75,907,810-77,647,496 , GRCh38 chr7: 76,440,557-78,180,243 PMS2P11, PTPN12, 32 more genes
    nsv3911276copy number variation1nstd102humanPathogenic GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085 POM121, GTF2IP1, 155 more genes
    nsv3909965copy number variation1nstd102humanUncertain significance NCBI36 chr7: 76,590,534-76,916,542 , GRCh37.p13 chr7: 76,752,598-77,078,606 , GRCh38.p12 chr7: 77,123,281-77,449,289 LOC102723791, GSAP, 4 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MNX1-AS2, VN1R31P, 2682 more genes
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