ndfip2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916819	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr13: 79,491,744-79,675,567 , NCBI36 chr13: 78,963,880-79,147,703 , GRCh37 chr13: 80,065,879-80,249,702	NDFIP2, LINC01068
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	NDFIP2, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	NDFIP2, LOC105370271, 925 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	NDFIP2, TEX30, 680 more genes
nsv3907697	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303	NDFIP2, GPC5, 565 more genes
nsv3898603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444	NDFIP2, RNY4P30, 575 more genes
nsv3918812	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 44,967,523-92,738,168 , NCBI36 chr13: 44,439,658-92,188,422 , GRCh37 chr13: 45,541,658-93,390,421	NDFIP2, SRSF1P1, 541 more genes
nsv6314117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618	NDFIP2, RBM26, 591 more genes
nsv3913649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 41,143,820-85,137,552 , GRCh37 chr13: 41,717,956-85,711,687 , NCBI36 chr13: 40,615,956-84,609,688	NDFIP2, RPL21P108, 539 more genes
nsv3882264	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 46,968,080-87,381,985 , GRCh37.p13 chr13: 47,542,215-88,034,240	NDFIP2, ARL11, 428 more genes
nsv4675995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857	NDFIP2, RNU7-88P, 396 more genes
nsv3895373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 57,058,434-94,684,615 , GRCh38.p12 chr13: 56,484,300-94,032,361	NDFIP2, LINC00383, 359 more genes
nsv3915859	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 47,117,587-84,300,935 , GRCh37 chr13: 47,691,722-84,875,070 , NCBI36 chr13: 46,589,723-83,773,071	NDFIP2, LOC105370231, 406 more genes
nsv6314171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258	NDFIP2, MIR4705, 430 more genes
nsv6291752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 59,574,760-89,410,027 , GRCh38.p12 chr13: 59,000,626-88,757,773	NDFIP2, GYG1P2, 284 more genes
nsv3913682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 61,110,478-85,127,323 , NCBI36 chr13: 60,008,479-84,025,324 , GRCh38 chr13: 60,536,344-84,553,188	NDFIP2, LOC105370251, 236 more genes
nsv3902290	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 61,686,543-83,302,092 , GRCh38.p12 chr13: 61,112,409-82,727,957	NDFIP2, LOC107987191, 216 more genes
nsv3918305	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 66,895,130-88,507,684 , GRCh38 chr13: 66,320,998-87,855,429 , NCBI36 chr13: 65,793,131-87,305,685	NDFIP2, LINC00397, 208 more genes
nsv3892831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 74,459,395-93,481,294 , GRCh38.p12 chr13: 73,885,258-92,829,041	NDFIP2, SPTLC1P5, 190 more genes
nsv3920687	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 77,821,262-94,152,099 , GRCh37 chr13: 78,923,261-95,354,098 , GRCh38 chr13: 78,349,126-94,701,844	NDFIP2, LINC00380, 145 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 74

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Number of Variants: 20

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Supplemental Content

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Search details

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