crim1[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
nsv3888258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 36,569,343-36,768,247 , GRCh38.p12 chr2: 36,342,200-36,541,104	CRIM1, CRIM1-DT
nsv4674332	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 36,521,758-36,589,156 , GRCh38.p12 chr2: 36,294,615-36,362,013 , GRCh38.p12 chr2\|NW_003315908.1: 1,303-74,734	CRIM1, CRIM1-DT, 1 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CRIM1, CYP1B1-AS1, 1649 more genes
nsv6313619	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300	CRIM1, LOC107985870, 161 more genes
nsv4454991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,940,473-36,813,297 , GRCh38.p12 chr2: 29,717,607-36,586,154	CRIM1, LOC105374435, 71 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	CRIM1, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	CRIM1, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	CRIM1, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	CRIM1, MTND2P22, 3724 more genes
nsv3908605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277	CRIM1, SLC35F6, 801 more genes
nsv3908288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875	CRIM1, ALLC, 674 more genes
nsv3875055	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850	CRIM1, RPL7P13, 426 more genes
nsv3879320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230	CRIM1, ATL2, 465 more genes
nsv3882842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406	CRIM1, STON1, 303 more genes
nsv6137788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145	CRIM1, GTF3C2-AS1, 316 more genes
nsv3877469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 28,069,882-43,543,420 , GRCh38.p12 chr2: 27,847,015-43,316,281	CRIM1, FOSL2, 219 more genes
nsv3911681	inversion	1	nstd102	human	Pathogenic	GRCh38.p12 chr2: 29,223,528-42,325,554 , GRCh37 chr2: 29,446,394-42,552,694	CRIM1, ALK, 163 more genes
nsv6112680	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882	CRIM1, ADCY3, 314 more genes
nsv3911624	inversion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr2: 29,224,814-42,327,254 , GRCh37 chr2: 29,447,680-42,554,394	CRIM1, ALK, 163 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	CRIM1, LOC101927723, 1246 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 22

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Number of Variants: 20

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Supplemental Content

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