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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097004copy number variation1nstd102humanUncertain significance GRCh37 chr4: 77,082,866-77,102,274 , GRCh38.p12 chr4: 76,161,713-76,181,121 SCARB2
    nsv7096867copy number variation1nstd102humanUncertain significance GRCh37 chr4: 77,116,840-77,134,696 , GRCh38.p12 chr4: 76,195,687-76,213,543 SCARB2, FAM47E
    nsv7052940inversion1nstd229human GRCh38 chr4: 73,455,263-76,320,440 , GRCh37.p13 chr4: 74,320,980-77,241,593 , RASSF6, 65 more genes
    nsv7048963inversion1nstd229human GRCh38 chr4: 76,206,957-76,207,396 , GRCh37.p13 chr4: 77,128,110-77,128,549 SCARB2
    nsv7043550inversion1nstd229human GRCh38 chr4: 76,204,026-76,207,091 , GRCh37.p13 chr4: 77,125,179-77,128,244 SCARB2
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6756935copy number variation1nstd229human GRCh38 chr4: 76,112,224-76,192,203 , GRCh37.p13 chr4: 77,033,377-77,113,356 ART3, NUP54, 1 more genes
    nsv6755415copy number variation1nstd229human GRCh38 chr4: 76,197,833-76,198,617 , GRCh37.p13 chr4: 77,118,986-77,119,770 SCARB2
    nsv6749694copy number variation1nstd229human GRCh38 chr4: 76,168,369-76,173,421 , GRCh37.p13 chr4: 77,089,522-77,094,574 SCARB2
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6744707copy number variation1nstd229human GRCh38 chr4: 76,205,462-76,745,563 , GRCh37.p13 chr4: 77,126,615-77,666,716 CCDC158, RNU6-1000P, 14 more genes
    nsv6743685copy number variation1nstd229human GRCh38 chr4: 76,191,804-76,294,018 , GRCh37.p13 chr4: 77,112,957-77,215,171 FAM47E-STBD1, LOC105377286, 2 more genes
    nsv6742320copy number variation1nstd229human GRCh38 chr4: 76,185,564-76,185,654 , GRCh37.p13 chr4: 77,106,717-77,106,807 SCARB2
    nsv6741352copy number variation1nstd229human GRCh38 chr4: 76,213,184-76,213,237 , GRCh37.p13 chr4: 77,134,337-77,134,390 SCARB2, FAM47E
    nsv6741224copy number variation1nstd229human GRCh38 chr4: 76,110,101-76,167,100 , GRCh37.p13 chr4: 77,031,254-77,088,253 SCARB2, NUP54, 1 more genes
    nsv6629735copy number variation1nstd224human GRCh37 chr4: 76,885,365-79,465,559 , GRCh38.p12 chr4: 75,964,212-78,544,405 CCNI, NUP54, 54 more genes
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6560852inversion1nstd223human GRCh38 chr4: 76,204,026-76,207,091 , GRCh37.p13 chr4: 77,125,179-77,128,244 SCARB2
    nsv6391489copy number variation1nstd223human GRCh38 chr4: 76,112,224-76,192,203 , GRCh37.p13 chr4: 77,033,377-77,113,356 SCARB2, NUP54, 1 more genes
    nsv6386773copy number variation1nstd223human GRCh38 chr4: 76,204,025-76,207,395 , GRCh37.p13 chr4: 77,125,178-77,128,548 SCARB2
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